[{"additionalPlain":"Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. \n","additional":"<div><em>Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees</em>.&nbsp;</div>","categories":{"commitment":"Full-Time - Remote","department":"Commercial","location":"Cambridge, MA","team":"Marketing","allLocations":["Cambridge, MA"]},"createdAt":1785273990460,"descriptionPlain":"Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at ScholarRock.com and follow @ScholarRock on X and on LinkedIn.\n \nSummary of Position:\n\n\nThis is an exciting opportunity for an experienced and passionate patient marketer to play a critical role in enabling the success of apitegromab, the company’s phase 3 candidate for the treatment of Spinal Muscular Atrophy (SMA). The Associate Director/Director of Patient Marketing will be a key member of the marketing team and will have the opportunity to help build a brand and patient strategy as well as shape and execute critical post launch tactics for apitegromab.\nThe primary responsibility of the Associate Director/Director of Patient Marketing will be to lead the non-personal promotion strategy and execution for patients inclusive of websites, media, and new digital  platforms/tactics ensuring a deeply patient-centric approach across education, engagement, and community presence. The role will lead the development of integrated, compliant, multi-channel patient programs designed to support awareness, understanding, and empowerment throughout the patient journey.\nReporting to the Senior Director of Patient Marketing, this individual will develop and execute an innovative multi-channel patient engagement plan working closely with Patient Services, Medical Affairs, Advocacy, Market Access, Legal, Regulatory, and Compliance to ensure a cohesive, high-quality experience for patients and caregivers. This is a high-impact, high-visibility role with the opportunity to help shape how Scholar Rock engages with the SMA community as it brings its first therapy to patients.\n","description":"<div><em>Scholar Rock is a late-stage <span data-ogsc=\"red\">global&nbsp;</span>biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity.&nbsp;Scholar Rock&nbsp;works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at </em><a rel=\"noopener noreferrer\" href=\"http://www.scholarrock.com/\" class=\"postings-link\"><em>ScholarRock.com</em></a><em> and follow </em><a rel=\"noopener noreferrer\" href=\"http://www.twitter.com/scholarrock\" class=\"postings-link\"><em>@ScholarRock</em></a><em> on X and on&nbsp;</em><a rel=\"noopener noreferrer\" href=\"https://www.linkedin.com/company/scholar-rock\" class=\"postings-link\"><em>LinkedIn</em></a><em>.</em></div>\n<div>&nbsp;</div>\n<div><strong style=\"font-size: 18px;\">Summary of Position:</strong></div><div><br></div><div>\n<p>This is an exciting opportunity for an experienced and passionate patient marketer to play a critical role in enabling the success of apitegromab, the company’s phase 3 candidate for the treatment of Spinal Muscular Atrophy (SMA). The Associate Director/Director of Patient Marketing will be a key member of the marketing team and will have the opportunity to help build a brand and patient strategy as well as shape and execute critical post launch tactics for apitegromab.</p>\n<p>The primary responsibility of the Associate Director/Director of Patient Marketing will be to lead the non-personal promotion strategy and execution for patients inclusive of websites, media, and new digital &nbsp;platforms/tactics ensuring a deeply patient-centric approach across education, engagement, and community presence. The role will lead the development of integrated, compliant, multi-channel patient programs designed to support awareness, understanding, and empowerment throughout the patient journey.</p>\n<p>Reporting to the Senior Director of Patient Marketing, this individual will develop and execute an innovative multi-channel patient engagement plan working closely with Patient Services, Medical Affairs, Advocacy, Market Access, Legal, Regulatory, and Compliance to ensure a cohesive, high-quality experience for patients and caregivers. This is a high-impact, high-visibility role with the opportunity to help shape how Scholar Rock engages with the SMA community as it brings its first therapy to patients.</p>\n</div>","id":"a5a52900-c834-49d9-8e3a-fe98fe3d1ec7","lists":[{"text":"Position Responsibilities: ","content":"<div>\n<p><strong>U.S. Patient Strategy &amp; Execution</strong></p>\n<ul type=\"disc\">\n<li>Develop and execute the end-to-end omni-channel strategy identifying business critical tactics to ensure post launch excellence</li>\n<li>Translate strategy into high-quality, compliant patient-facing tactics, owning the execution of all non-personal promotion, inclusive of unbranded and branded websites, media, social media, and CRM</li>\n<li>Optimize digital performance through analytics and audience insights, and maximize ROI across paid, owned and earned digital channels.</li>\n<li>Lead the strategy and execution of new digital platforms, which may include, but is not limited to YouTube, Reddit, Apps, or innovative digital partnerships</li>\n<li>Ensure consistency and excellence across all patient touchpoints while maintaining a strong, authentic patient-centric lens.</li>\n\n<p><strong>Patient Engagement &amp; Community Leadership</strong></p>\n<ul type=\"disc\">\n<li>Build and maintain strong, trusted relationships within the SMA patient and caregiver community.</li>\n<li>Partner with Patient Advocacy and the Patient Relationship agency to ensure patient feedback is incorporated and the patient voice is represented and accurately reflected in patient materials</li>\n<li>Champion innovation in patient engagement, continuously evolving approaches to improve the patient experience across the journey.</li>\n\n<p><strong>Cross-Functional Leadership</strong></p>\n<ul type=\"disc\">\n<li>Serve as a core member of the U.S. Marketing Team, partnering closely with Patient Services, Medical Affairs, Advocacy, Market Access, Regulatory, Legal, and Compliance.</li>\n<li>Ensure strong alignment between patient marketing initiatives and patient support programs, including development of branded patient materials.</li>\n<li>Clearly communicate and champion patient brand strategy with internal stakeholders and external partners.</li>\n\n<p><strong>Agency, Budget &amp; Operational Excellence</strong></p>\n<ul type=\"disc\">\n<li>Partner with agency-of-record and media agency to deliver high impact patient marketing initiatives, driving strategic value, innovation, and executional excellence.</li>\n<li>Lead the development of patient-facing assets, event kits, and materials to support consistent execution across the field.</li>\n<li>Ability to prioritize post launch critical tactics and optimization of the budget, demonstrating strong fiscal discipline and accountability.</li>\n<li>Support post launch readiness, participate in promotional review processes, and ongoing optimization of patient tactics.</li>\n\n</ul></ul></ul></ul></div>"},{"text":"Candidate Requirements: ","content":"<div>\n<ul type=\"disc\">\n<li>Bachelor’s degree required; advanced degree preferred.</li>\n<li>6+ years of experience in pharmaceutical or biotechnology marketing, with significant experience in U.S. patient/consumer marketing.</li>\n<li>6+ years of experience leading the development and execution of integrated digital marketing strategies creating compliant, data-driven campaigns that increased patient engagement</li>\n<li>Demonstrated success leading patient marketing strategy and execution in specialty or rare disease environments.</li>\n<li>Experience in neurology, neuromuscular disease, or rare disease strongly preferred.</li>\n<li>Deep commitment to patient centricity with the ability to translate insight into impactful, compliant engagement.</li>\n<li>Strong understanding of regulatory, legal, and compliance requirements for patient-facing communications.</li>\n<li>Proven ability to lead agencies, manage budgets, and operate effectively in a matrixed organization.</li>\n<li>Excellent communication, influence, and stakeholder-management skills.</li>\n<li>Entrepreneurial mindset with comfort operating in a first-launch, high-growth environment.</li>\n<li>Willingness to travel as needed (anticipated up to ~30%).</li>\n\n</ul></div>"}],"salaryRange":{"min":175000,"max":260000,"currency":"USD","interval":"per-year-salary"},"text":"Associate Director/Director, Patient Marketing (US)","country":"US","workplaceType":"remote","opening":"<div><em>Scholar Rock is a late-stage <span data-ogsc=\"red\">global&nbsp;</span>biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity.&nbsp;Scholar Rock&nbsp;works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at </em><a class=\"postings-link\" href=\"http://www.scholarrock.com/\" target=\"_blank\" rel=\"noopener noreferrer\"><em>ScholarRock.com</em></a><em> and follow </em><a class=\"postings-link\" href=\"http://www.twitter.com/scholarrock\" target=\"_blank\" rel=\"noopener noreferrer\"><em>@ScholarRock</em></a><em> on X and on&nbsp;</em><a class=\"postings-link\" href=\"https://www.linkedin.com/company/scholar-rock\" target=\"_blank\" rel=\"noopener noreferrer\"><em>LinkedIn</em></a><em>.</em></div>\n<div>&nbsp;</div>\n<div><strong style=\"font-size: 18px;\">Summary of Position:</strong></div>","openingPlain":"Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at ScholarRock.com and follow @ScholarRock on X and on LinkedIn.\n \nSummary of Position:\n","descriptionBody":"<div>\n<p>This is an exciting opportunity for an experienced and passionate patient marketer to play a critical role in enabling the success of apitegromab, the company&rsquo;s phase 3 candidate for the treatment of Spinal Muscular Atrophy (SMA). The Associate Director/Director of Patient Marketing will be a key member of the marketing team and will have the opportunity to help build a brand and patient strategy as well as shape and execute critical post launch tactics for apitegromab.</p>\n<p>The primary responsibility of the Associate Director/Director of Patient Marketing will be to lead the non-personal promotion strategy and execution for patients inclusive of websites, media, and new digital &nbsp;platforms/tactics ensuring a deeply patient-centric approach across education, engagement, and community presence. The role will lead the development of integrated, compliant, multi-channel patient programs designed to support awareness, understanding, and empowerment throughout the patient journey.</p>\n<p>Reporting to the Senior Director of Patient Marketing, this individual will develop and execute an innovative multi-channel patient engagement plan working closely with Patient Services, Medical Affairs, Advocacy, Market Access, Legal, Regulatory, and Compliance to ensure a cohesive, high-quality experience for patients and caregivers. This is a high-impact, high-visibility role with the opportunity to help shape how Scholar Rock engages with the SMA community as it brings its first therapy to patients.</p>\n</div>","descriptionBodyPlain":"This is an exciting opportunity for an experienced and passionate patient marketer to play a critical role in enabling the success of apitegromab, the company’s phase 3 candidate for the treatment of Spinal Muscular Atrophy (SMA). The Associate Director/Director of Patient Marketing will be a key member of the marketing team and will have the opportunity to help build a brand and patient strategy as well as shape and execute critical post launch tactics for apitegromab.\nThe primary responsibility of the Associate Director/Director of Patient Marketing will be to lead the non-personal promotion strategy and execution for patients inclusive of websites, media, and new digital  platforms/tactics ensuring a deeply patient-centric approach across education, engagement, and community presence. The role will lead the development of integrated, compliant, multi-channel patient programs designed to support awareness, understanding, and empowerment throughout the patient journey.\nReporting to the Senior Director of Patient Marketing, this individual will develop and execute an innovative multi-channel patient engagement plan working closely with Patient Services, Medical Affairs, Advocacy, Market Access, Legal, Regulatory, and Compliance to ensure a cohesive, high-quality experience for patients and caregivers. This is a high-impact, high-visibility role with the opportunity to help shape how Scholar Rock engages with the SMA community as it brings its first therapy to patients.\n","hostedUrl":"https://jobs.lever.co/scholarrock/a5a52900-c834-49d9-8e3a-fe98fe3d1ec7","applyUrl":"https://jobs.lever.co/scholarrock/a5a52900-c834-49d9-8e3a-fe98fe3d1ec7/apply"},{"additionalPlain":"Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. \n","additional":"<div><em>Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees</em>.&nbsp;</div>","categories":{"commitment":"Full-Time","department":"Commercial","location":"Cambridge, MA","team":"Commercial Operations","allLocations":["Cambridge, MA"]},"createdAt":1785845853995,"descriptionPlain":"Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at ScholarRock.com and follow @ScholarRock on X and on LinkedIn.\n \nSummary of Position:\n\n\nThe Director, Meetings & Events is responsible for leading the planning and execution of Scholar Rock’s congresses, medical and commercial meetings, and internal events. This role partners closely with Commercial, Medical Affairs, Legal, Compliance, Finance, and external vendors to deliver high-quality, compliant, and impactful events that support the company’s strategic objectives.\nBased on the annual event calendar and business priorities, the Director will manage a portfolio of assigned events, providing end-to-end leadership across planning, execution, budgeting, compliance, and post-event evaluation. In addition, this role will help drive operational excellence by supporting financial tracking, process improvement, and strategic meeting operations across the organization.\n","description":"<div><em>Scholar Rock is a late-stage <span data-ogsc=\"red\">global&nbsp;</span>biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity.&nbsp;Scholar Rock&nbsp;works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at </em><a rel=\"noopener noreferrer\" href=\"http://www.scholarrock.com/\" class=\"postings-link\"><em>ScholarRock.com</em></a><em> and follow </em><a rel=\"noopener noreferrer\" href=\"http://www.twitter.com/scholarrock\" class=\"postings-link\"><em>@ScholarRock</em></a><em> on X and on&nbsp;</em><a rel=\"noopener noreferrer\" href=\"https://www.linkedin.com/company/scholar-rock\" class=\"postings-link\"><em>LinkedIn</em></a><em>.</em></div>\n<div>&nbsp;</div>\n<div><strong style=\"font-size: 18px;\">Summary of Position:</strong></div><div><br></div><div>\n<p>The Director, Meetings &amp; Events is responsible for leading the planning and execution of Scholar Rock’s congresses, medical and commercial meetings, and internal events. This role partners closely with Commercial, Medical Affairs, Legal, Compliance, Finance, and external vendors to deliver high-quality, compliant, and impactful events that support the company’s strategic objectives.</p>\n<p>Based on the annual event calendar and business priorities, the Director will manage a portfolio of assigned events, providing end-to-end leadership across planning, execution, budgeting, compliance, and post-event evaluation. In addition, this role will help drive operational excellence by supporting financial tracking, process improvement, and strategic meeting operations across the organization.</p>\n</div>","id":"4c9a86cc-5f40-42d1-ad65-d58320eb7d7d","lists":[{"text":"Position Responsibilities: ","content":"<div>\n<p><strong>Strategic Partnership &amp; Stakeholder Management</strong></p>\n<ul type=\"disc\">\n<li>Serve as a trusted partner to Commercial, Medical Affairs, and cross-functional stakeholders to understand event objectives and deliver exceptional meeting experiences.</li>\n<li>Foster strong working relationships across internal teams to ensure alignment on event strategy, timelines, budgets, and execution plans.</li>\n<li>Collaborate closely with Legal, Compliance and Finance to ensure adherence to company policies and industry regulations.</li>\n\n<p><strong>Meeting &amp; Congress Planning</strong></p>\n<ul type=\"disc\">\n<li>Lead the planning and execution of assigned US and Global congresses, national meetings, and internal corporate events.</li>\n<li>Manage all event logistics including venue selection, transportation, catering, room layouts, registration, housing, audiovisual services, and attendee communications.</li>\n<li>Provide end-to-end management of smaller standalone meetings and ancillary events as required.</li>\n\n<p><strong>Budget &amp; Financial Management</strong></p>\n<ul type=\"disc\">\n<li>Develop and manage event budgets while ensuring cost-effective execution and alignment with organizational goals.</li>\n<li>Track expenses, process invoices, and maintain accurate financial reporting for assigned programs.</li>\n<li>Partner with Finance and leadership to support forecasting, reconciliation, and budget planning activities.</li>\n\n<p><strong>Vendor &amp; Agency Management</strong></p>\n<ul type=\"disc\">\n<li>Manage relationships with meeting agencies, congress partners, venues, and third-party vendors.</li>\n<li>Support vendor selection, contract negotiation, and performance management to ensure service excellence and value optimization.</li>\n<li>Ensure vendors meet established quality, compliance, and operational standards.</li>\n\n<p><strong>Event Operations &amp; Execution</strong></p>\n<ul type=\"disc\">\n<li>Oversee event readiness, including development of agendas, meeting materials, registration processes, attendee management, and onsite logistics.</li>\n<li>Provide onsite leadership for key events, ensuring seamless execution and rapid resolution of operational issues.</li>\n<li>Coordinate booth management, meeting room operations, speaker support, registration services, and event teardown activities.</li>\n\n<p><strong>Communications &amp; Attendee Experience</strong></p>\n<ul type=\"disc\">\n<li>Partner with Commercial and Medical teams to support attendee communications, event promotions, and registration campaigns.</li>\n<li>Ensure all stakeholder and attendee communications are timely, accurate, and aligned with event objectives.</li>\n<li>Deliver a best-in-class attendee experience across all meetings and events.</li>\n\n<p><strong>Compliance &amp; Risk Management</strong></p>\n<ul type=\"disc\">\n<li>Ensure all meetings and events comply with applicable healthcare regulations, industry guidelines, company policies, and HCP spending requirements.</li>\n<li>Partner with Compliance to monitor event activities and maintain appropriate documentation, approvals, and reporting.</li>\n<li>Identify and mitigate operational and compliance risks throughout the planning process.</li>\n\n<p><strong>Continuous Improvement &amp; Reporting</strong></p>\n<ul type=\"disc\">\n<li>Conduct post-event evaluations and gather stakeholder feedback to measure outcomes and identify opportunities for improvement.</li>\n<li>Analyze event metrics, attendee engagement, and operational performance to enhance future programs.</li>\n<li>Contribute to the development of scalable processes, tools, and best practices that improve the effectiveness of the Meetings &amp; Events function.</li>\n\n</ul></ul></ul></ul></ul></ul></ul></ul></div>"},{"text":"Candidate Requirements:","content":"<div>\n<ul type=\"disc\">\n<li>Bachelor's degree in Hospitality Management, Event Management, Marketing, Communications, Business Administration, or a related field required.</li>\n\n<ul type=\"disc\">\n<li>Minimum of 7 years of experience planning and executing meetings, congresses, and events in the pharmaceutical, biotechnology, or healthcare industry.</li>\n<li>Demonstrated success managing global events and working with international stakeholders and vendors.</li>\n\n<ul type=\"disc\">\n<li>Certified Meeting Professional (CMP), CMP-HC, Certified Meeting Manager (CMM), or similar certification preferred.</li>\n\n<ul type=\"disc\">\n<li>Proficiency with Microsoft Office Suite, including Excel and PowerPoint.</li>\n<li>Experience with event management platforms such as Cvent, ExhibitForce, or equivalent meeting technologies.</li>\n\n\n<li>Familiarity with budget management, registration systems, and event analytics tools.</li>\n\n<ul type=\"disc\">\n<li>Strong ability to influence and collaborate across diverse stakeholder groups in a fast-paced environment.</li>\n<li>Demonstrated success managing complex, cross-functional initiatives with multiple priorities.</li>\n\n<ul type=\"disc\">\n<li>Exceptional organizational and project management skills with the ability to manage multiple events simultaneously.</li>\n<li>Proven ability to prioritize work, meet deadlines, and deliver results under pressure.</li>\n\n<ul type=\"disc\">\n<li>Outstanding verbal, written, and interpersonal communication skills.</li>\n<li>Ability to engage effectively with senior leaders, healthcare professionals, vendors, and cross-functional teams.</li>\n\n<ul type=\"disc\">\n<li>Resourceful and proactive approach to addressing challenges and resolving issues quickly and effectively.</li>\n\n<ul type=\"disc\">\n<li>Experience negotiating vendor contracts and managing event budgets to maximize value and achieve business objectives.</li>\n\n<ul type=\"disc\">\n<li>Strong attention to detail with a commitment to operational excellence and flawless execution.</li>\n\n<ul type=\"disc\">\n<li><span data-teams=\"true\">Demonstrated success managing global events and working with international stakeholders and vendors</span></li>\n<li>Additional language proficiency is valued but not required.</li>\n\n</ul></ul></ul></ul></ul></ul></ul></ul></ul></ul></ul></div>"}],"salaryRange":{"min":200000,"max":250000,"currency":"USD","interval":"per-year-salary"},"text":"Director, Meetings & Events","country":"US","workplaceType":"remote","opening":"<div><em>Scholar Rock is a late-stage <span data-ogsc=\"red\">global&nbsp;</span>biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity.&nbsp;Scholar Rock&nbsp;works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at </em><a class=\"postings-link\" href=\"http://www.scholarrock.com/\" target=\"_blank\" rel=\"noopener noreferrer\"><em>ScholarRock.com</em></a><em> and follow </em><a class=\"postings-link\" href=\"http://www.twitter.com/scholarrock\" target=\"_blank\" rel=\"noopener noreferrer\"><em>@ScholarRock</em></a><em> on X and on&nbsp;</em><a class=\"postings-link\" href=\"https://www.linkedin.com/company/scholar-rock\" target=\"_blank\" rel=\"noopener noreferrer\"><em>LinkedIn</em></a><em>.</em></div>\n<div>&nbsp;</div>\n<div><strong style=\"font-size: 18px;\">Summary of Position:</strong></div>","openingPlain":"Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at ScholarRock.com and follow @ScholarRock on X and on LinkedIn.\n \nSummary of Position:\n","descriptionBody":"<div>\n<p>The Director, Meetings &amp; Events is responsible for leading the planning and execution of Scholar Rock&rsquo;s congresses, medical and commercial meetings, and internal events. This role partners closely with Commercial, Medical Affairs, Legal, Compliance, Finance, and external vendors to deliver high-quality, compliant, and impactful events that support the company&rsquo;s strategic objectives.</p>\n<p>Based on the annual event calendar and business priorities, the Director will manage a portfolio of assigned events, providing end-to-end leadership across planning, execution, budgeting, compliance, and post-event evaluation. In addition, this role will help drive operational excellence by supporting financial tracking, process improvement, and strategic meeting operations across the organization.</p>\n</div>","descriptionBodyPlain":"The Director, Meetings & Events is responsible for leading the planning and execution of Scholar Rock’s congresses, medical and commercial meetings, and internal events. This role partners closely with Commercial, Medical Affairs, Legal, Compliance, Finance, and external vendors to deliver high-quality, compliant, and impactful events that support the company’s strategic objectives.\nBased on the annual event calendar and business priorities, the Director will manage a portfolio of assigned events, providing end-to-end leadership across planning, execution, budgeting, compliance, and post-event evaluation. In addition, this role will help drive operational excellence by supporting financial tracking, process improvement, and strategic meeting operations across the organization.\n","hostedUrl":"https://jobs.lever.co/scholarrock/4c9a86cc-5f40-42d1-ad65-d58320eb7d7d","applyUrl":"https://jobs.lever.co/scholarrock/4c9a86cc-5f40-42d1-ad65-d58320eb7d7d/apply"},{"additionalPlain":"Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. \n","additional":"<div><em>Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees</em>.&nbsp;</div>","categories":{"commitment":"Full-Time","department":"G&A","location":"Cambridge, MA","team":"Information Technology","allLocations":["Cambridge, MA"]},"createdAt":1786469959851,"descriptionPlain":"Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at ScholarRock.com and follow @ScholarRock on X and on LinkedIn.\n \nSummary of Position:\n\n\nScholar Rock is seeking a Director of Research and Development Technology to cultivate strong functional partnerships to develop strategic solutions to Scholar Rock’s growing research and development pipeline.  This position, reporting to the Chief Information Officer, is a pivotal role in the IT organization as the company transitions to a global commercial operation.  In this role, you will lead the strategy, delivery, and manage the lifecycle of IT systems across Research, Clinical Development, Regulatory, and Pharmacovigilance.  In addition, the Director will develop and lead the Laboratory of the Future initiative to incubate the usage of Artificial Intelligence, Robotics, and Data Science.\n\nThis role requires a dynamic and passionate individual, combining strategic business partnership with hands-on support in conjunction with our managed service provider.\n \n \n \n \n \n \nPosition Responsibilities \n","description":"<div><em>Scholar Rock is a late-stage <span data-ogsc=\"red\">global&nbsp;</span>biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity.&nbsp;Scholar Rock&nbsp;works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at </em><a rel=\"noopener noreferrer\" href=\"http://www.scholarrock.com/\" class=\"postings-link\"><em>ScholarRock.com</em></a><em> and follow </em><a rel=\"noopener noreferrer\" href=\"http://www.twitter.com/scholarrock\" class=\"postings-link\"><em>@ScholarRock</em></a><em> on X and on&nbsp;</em><a rel=\"noopener noreferrer\" href=\"https://www.linkedin.com/company/scholar-rock\" class=\"postings-link\"><em>LinkedIn</em></a><em>.</em></div>\n<div>&nbsp;</div>\n<div><strong style=\"font-size: 18px;\">Summary of Position:</strong></div><div><br></div><div>Scholar Rock is seeking a Director of Research and Development Technology to cultivate strong functional partnerships to develop strategic solutions to Scholar Rock’s growing research and development pipeline. &nbsp;This position, reporting to the Chief Information Officer, is a pivotal role in the IT organization as the company transitions to a global commercial operation. &nbsp;In this role, you will lead the strategy, delivery, and manage the lifecycle of IT systems across Research, Clinical Development, Regulatory, and Pharmacovigilance. &nbsp;In addition, the Director will develop and lead the Laboratory of the Future initiative to incubate the usage of Artificial Intelligence, Robotics, and Data Science.</div>\n<div><br>This role requires a dynamic and passionate individual, combining strategic business partnership with hands-on support in conjunction with our managed service provider.</div>\n<div>&nbsp;</div>\n<div>&nbsp;</div>\n<div>&nbsp;</div>\n<div>&nbsp;</div>\n<div>&nbsp;</div>\n<div>&nbsp;</div>\n<h3>Position Responsibilities&nbsp;</h3>","id":"7aa3ac2f-dfaf-4a7d-9ca4-da6a20df9213","lists":[{"text":"Strategic Development Business Partnership","content":"\n<li>Serve as the lead IT partner across Clinical Operations, Data Management, and Biometrics</li>\n<li>Translate scientific, regulatory, CMC, and safety strategy into a multi-year development digital roadmap</li>\n<li>Partner with executive leaders across R&amp;D, CMC, Regulatory, Safety, and Quality to identify opportunities where technology, data, and AI accelerate decision-making, improve compliance, and reduce cycle time</li>\n<li>Represent IT within Development leadership forums and influence enterprise strategy across the product lifecycle</li>\n"},{"text":"Development Domain Architecture & Application Strategy","content":"\n<li>Own the technical architecture across Scholar Rock’s Development digital ecosystem, including scientific research, translational sciences, preclinical, R&amp;D operations, CMC, Regulatory, and Safety systems</li>\n<li>Ensure systems, data, and AI capabilities scale with Scholar Rock’s pipeline, regulatory expectations, and global operating footprint</li>\n<li>Lead lifecycle management of scientific, regulatory, safety, and CMC applications</li>\n<li>Define architectural standards, integration patterns, master data models, and interoperability across scientific, regulatory, safety, CMC, and enterprise systems</li>\n<li>Partner with Enterprise Applications, Cybersecurity, and Network Platform Engineering to ensure Development platforms are secure, reliable, and aligned with enterprise standards</li>\n"},{"text":"R&D, Translational & Preclinical Enablement","content":"\n<li>Provide architecture and delivery leadership for research, translational, preclinical, and R&amp;D operations</li>\n<li>Support biomarker development, PK/PD workflows, in vivo studies, and translational analytics</li>\n<li>Support imaging, omics, and high-content workflows where applicable</li>\n"},{"text":"CMC Technology Enablement","content":"\n<li>Own technology capabilities supporting CMC development, process development, analytical development, and CMC operations</li>\n<li>Enable technology continuity across R&amp;D → CMC transitions</li>\n<li>Partner with Quality and Manufacturing Technology on validated systems, data integrity, and lifecycle continuity</li>\n"},{"text":"Regulatory & Safety Technology","content":"\n<li>Own technology strategy and delivery for Regulatory Affairs, Safety, and Medical Writing platforms, including RIM, safety systems, submission platforms, and document management</li>\n<li>Ensure systems and data support inspection readiness, submission planning, safety case management, and lifecycle management</li>\n<li>Partner with Regulatory, Safety, and Quality to ensure global compliance and audit readiness</li>\n"},{"text":"Data, AI & Scientific Computing","content":"\n<li>Partner with Enterprise Data &amp; AI to define data flows across R&amp;D, CMC, Regulatory, and Safety into Scholar Rock’s enterprise data platform</li>\n<li>Enable structured data products for scientific, translational, regulatory, CMC, and safety domains</li>\n<li>Partner with Enterprise Data &amp; AI to design and operationalize generative and agentic AI capabilities across development workflows</li>\n<li>Architect secure scientific computing environments and Trusted Research Environments (TREs) to support sensitive datasets and controlled access</li>\n<li>Enable responsible AI practices for development use cases</li>\n"},{"text":"External R&D + CMC Ecosystem Enablement","content":"\n<li>Partner with R&amp;D Operations and CMC leaders to enable seamless collaboration with CROs, CDMOs, contract testing labs, and academic collaborators</li>\n<li>Define secure data exchange models, validated interfaces, and vendor connectivity patterns</li>\n<li>Support the operating model for external partner integrations, including data ingestion, workflow interoperability, and validated interfaces</li>\n"},{"text":"Cross-Lifecycle Alignment","content":"\n<li>Partner with Research, Development, CMC, Regulatory, Safety, and Quality to ensure digital capabilities support scientific and portfolio priorities across the product lifecycle</li>\n<li>Provide architecture guidance for cross-functional lifecycle data continuity across Discovery → Clinical → CMC → Regulatory → Safety</li>\n<li>Enable seamless data exchange, workflow interoperability, and validated interfaces across development-adjacent functions</li>\n"},{"text":"Delivery, Governance & Operating Model","content":"\n<li>Establish and mature the Development IT operating model, including product management, engineering, application support, vendor management, and validation</li>\n<li>Establish governance and standards for validation, GxP/GLP, data integrity, information security, and audit readiness</li>\n<li>Own delivery of Development IT initiatives, ensuring scope, quality, cost, timeline, and risk are actively managed</li>\n<li>Serve as the executive escalation point for R&amp;D, CMC, Regulatory, and Safety technology issues and delivery risks</li>\n"},{"text":"Cross-Functional Partnership","content":"\n<li>\n<p>Partner with Enterprise Data &amp; AI, Enterprise Applications, Network Platform Engineering, Cybersecurity, Digital Workplace, and Quality/CSV to ensure Development platforms are integrated, secure, reliable, and compliant</p>\n</li>\n<li>\n<p>&nbsp;</p>\n<p>&nbsp;</p>\nPartner with Procurement, Finance, and Legal on vendor selection, contracts, and cost governance</li>\n"},{"text":"Team & Talent Leadership","content":"\n<li>Build and develop a high-performing Development IT team, including product management, business analysis, architecture, engineering, and application support</li>\n<li>Foster a culture of scientific curiosity, delivery excellence, compliance rigor, and pragmatic problem-solving</li>\n<li>Establish talent, growth, and capability development paths as the function scales</li>\n"},{"text":"Candidate Requirements","content":"\n<li>Bachelor’s degree in Computer Science, Engineering, Data Science, Life Sciences, or related field (or equivalent experience)</li>\n<li>10+ years of progressive IT leadership supporting Development functions including R&amp;D, CMC, Regulatory, or Safety in biotech or pharma</li>\n<li>Demonstrated architectural depth across scientific, CMC, regulatory, or safety systems</li>\n<li>Demonstrated business partnership with senior scientific, CMC, regulatory, safety, and quality leaders</li>\n<li>Strong understanding of GxP, GLP, CSV, data integrity, and regulated life sciences environments</li>\n<li>Experience integrating domain systems with enterprise data platforms (e.g., Snowflake, Databricks) in partnership with centralized teams</li>\n<li>Practical experience applying modern data engineering, generative AI, and agentic AI in life sciences environments</li>\n<li>Excellent executive communication and stakeholder-management skills</li>\n"}],"salaryRange":{"min":200000,"max":260000,"currency":"USD","interval":"per-year-salary"},"text":"Director, Research & Development Technology","country":"US","workplaceType":"onsite","opening":"<div><em>Scholar Rock is a late-stage <span data-ogsc=\"red\">global&nbsp;</span>biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity.&nbsp;Scholar Rock&nbsp;works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at </em><a class=\"postings-link\" href=\"http://www.scholarrock.com/\" target=\"_blank\" rel=\"noopener noreferrer\"><em>ScholarRock.com</em></a><em> and follow </em><a class=\"postings-link\" href=\"http://www.twitter.com/scholarrock\" target=\"_blank\" rel=\"noopener noreferrer\"><em>@ScholarRock</em></a><em> on X and on&nbsp;</em><a class=\"postings-link\" href=\"https://www.linkedin.com/company/scholar-rock\" target=\"_blank\" rel=\"noopener noreferrer\"><em>LinkedIn</em></a><em>.</em></div>\n<div>&nbsp;</div>\n<div><strong style=\"font-size: 18px;\">Summary of Position:</strong></div>","openingPlain":"Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at ScholarRock.com and follow @ScholarRock on X and on LinkedIn.\n \nSummary of Position:\n","descriptionBody":"<div>Scholar Rock is seeking a Director of Research and Development Technology to cultivate strong functional partnerships to develop strategic solutions to Scholar Rock&rsquo;s growing research and development pipeline. &nbsp;This position, reporting to the Chief Information Officer, is a pivotal role in the IT organization as the company transitions to a global commercial operation. &nbsp;In this role, you will lead the strategy, delivery, and manage the lifecycle of IT systems across Research, Clinical Development, Regulatory, and Pharmacovigilance. &nbsp;In addition, the Director will develop and lead the Laboratory of the Future initiative to incubate the usage of Artificial Intelligence, Robotics, and Data Science.</div>\n<div><br>This role requires a dynamic and passionate individual, combining strategic business partnership with hands-on support in conjunction with our managed service provider.</div>\n<div>&nbsp;</div>\n<div>&nbsp;</div>\n<div>&nbsp;</div>\n<div>&nbsp;</div>\n<div>&nbsp;</div>\n<div>&nbsp;</div>\n<h3>Position Responsibilities&nbsp;</h3>","descriptionBodyPlain":"Scholar Rock is seeking a Director of Research and Development Technology to cultivate strong functional partnerships to develop strategic solutions to Scholar Rock’s growing research and development pipeline.  This position, reporting to the Chief Information Officer, is a pivotal role in the IT organization as the company transitions to a global commercial operation.  In this role, you will lead the strategy, delivery, and manage the lifecycle of IT systems across Research, Clinical Development, Regulatory, and Pharmacovigilance.  In addition, the Director will develop and lead the Laboratory of the Future initiative to incubate the usage of Artificial Intelligence, Robotics, and Data Science.\n\nThis role requires a dynamic and passionate individual, combining strategic business partnership with hands-on support in conjunction with our managed service provider.\n \n \n \n \n \n \nPosition Responsibilities \n","hostedUrl":"https://jobs.lever.co/scholarrock/7aa3ac2f-dfaf-4a7d-9ca4-da6a20df9213","applyUrl":"https://jobs.lever.co/scholarrock/7aa3ac2f-dfaf-4a7d-9ca4-da6a20df9213/apply"},{"additionalPlain":"Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. \n","additional":"<div><em>Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees</em>.&nbsp;</div>","categories":{"commitment":"Full-Time","department":"Technical Operations","location":"Tokyo","team":"Manufacturing & Supply Chain","allLocations":["Tokyo"]},"createdAt":1782830067397,"descriptionPlain":"Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at ScholarRock.com and follow @ScholarRock on X and on LinkedIn.\n \nSummary of Position:\n\n\nThe Director of Supply Chain is responsible for building, implementing, and managing the commercial supply chain for Scholar Rock in Japan. The role will oversee daily operations relating to artwork, secondary packaging and distribution activities and will work closely with Scholar Rock colleagues globally, primarily in the US and Ireland. The position requires strong leadership, problem-solving, and analytical skills to optimize operational efficiency, reduce costs, and ensure products are reliably and compliantly supplied across Japan.\n","description":"<div><em>Scholar Rock is a late-stage <span data-ogsc=\"red\">global&nbsp;</span>biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity.&nbsp;Scholar Rock&nbsp;works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at </em><a rel=\"noopener noreferrer\" href=\"http://www.scholarrock.com/\" class=\"postings-link\"><em>ScholarRock.com</em></a><em> and follow </em><a rel=\"noopener noreferrer\" href=\"http://www.twitter.com/scholarrock\" class=\"postings-link\"><em>@ScholarRock</em></a><em> on X and on&nbsp;</em><a rel=\"noopener noreferrer\" href=\"https://www.linkedin.com/company/scholar-rock\" class=\"postings-link\"><em>LinkedIn</em></a><em>.</em></div>\n<div>&nbsp;</div>\n<div><strong style=\"font-size: 18px;\">Summary of Position:</strong></div><div><br></div><div>\n<p style=\"text-align: justify; margin: 0in; font-size: 12pt; font-family: Cambria, serif;\"><span style=\"font-size: 10.0pt; font-family: Arial, sans-serif;\">The Director of Supply Chain is responsible for building, implementing, and managing the commercial supply chain for Scholar Rock in Japan. The role will oversee daily operations relating to artwork, secondary packaging and distribution activities and will work closely with Scholar Rock colleagues globally, primarily in the US and Ireland. </span><span style=\"font-size: 10.0pt; font-family: Arial, sans-serif;\">The position requires strong leadership, problem-solving, and analytical skills to optimize operational efficiency, reduce costs, and ensure products are reliably and compliantly supplied across Japan.</span></p>\n</div>","id":"279d2e8f-5901-4819-911d-0a64b720ed90","lists":[{"text":" Position Responsibilities: ","content":"<div>\n<p>Strategic Leadership</p>\n<ul type=\"disc\">\n<li>Manage the end-to-end supply chain operations: Establish strategies and oversee launch execution.</li>\n<li>Drive strategic capabilities: Establish strong capabilities to support current and future assets resulting from the Scholar Rock pipeline.</li>\n<li>Foster cross-departmental collaboration: Work closely with departments such as planning, manufacturing, logistics, regulatory, finance, IT and commercial teams to ensure supply objectives align with broader business priorities.</li>\n\n<p>&nbsp;</p>\n<p>External Partner Relationship Management</p>\n<ul type=\"disc\">\n<li>Establish and strengthen external partnerships: Build and sustain productive relationships with external packaging contract manufacturers (CMOs) ensuring mutual benefits in terms of efficiency and cost savings.</li>\n<li>Negotiate and secure strategic contracts: Support contract negotiations with packaging CMO providers to secure favorable terms and maintain high-quality service delivery.</li>\n<li>Lead New Product Introduction execution with external partners for Japanese market</li>\n<li>Packaging qualification: Oversight of product packaging qualification and validations activities to ensure compliance with regulations.</li>\n<li>Coordinate logistics operations with colleagues and partners on the importation of drug product, and the transfer of finished goods to Wholesalers.</li>\n<li>Continuous Improvement: Support continuous performance assessment and utilization of KPIs of CMO partners regarding compliance, pricing, service and capacity while maintaining business review meetings.</li>\n<li>Risk mitigation: Design, implement and monitor supply operations risk mitigation strategies.</li>\n\n<p>&nbsp;</p>\n<p>Supply Chain Systems</p>\n<ul type=\"disc\">\n<li>Supply System readiness: Partner with IT to implement systems to support supply chain operations in compliance with regulatory requirements.</li>\n<li>Materials Management: Oversee purchase order/invoice management and material management within the Scholar Rock ERP system for Japan.</li>\n\n<p>&nbsp;</p>\n<p>Budgeting, Cost Control &amp; Financial Oversight</p>\n<ul type=\"disc\">\n<li>Champion budgeting &amp; cost control: Support management of the supply chain operations budget, monitor expenses, and actively identify opportunities for cost reduction while maintaining high service quality standards.</li>\n<li>Conduct strategic cost-benefit analysis: Support in-depth analysis of supply chain operations to uncover potential savings in operational efficiency.</li>\n\n<p>&nbsp;</p>\n<p>Delivery &amp; Customer Satisfaction</p>\n<ul type=\"disc\">\n<li>Drive timely product supply: Ensure that the inventory supply runs smoothly, meeting product delivery timelines and customer expectations.</li>\n<li>Ensure customer satisfaction: Guarantee timely and accurate product deliveries while maintaining service quality, accuracy, and attention to customer needs.</li>\n<li>Resolve supply operations issues: Address and resolve product supply issues related to packaging operations or operational challenges to maintain high levels of customer satisfaction and service excellence.</li>\n\n<p>&nbsp;</p>\n<p>Organizational &amp; Cross Functional Leadership</p>\n<ul type=\"disc\">\n<li>Be a proactive member of the supply chain and Japanese teams to drive commercial success.</li>\n<li>Collaborate closely with global execution teams (IT/Systems, Finance) to ensure cross functional alignment.</li>\n<li>Partner with quality and regulatory teams to ensure compliance with global regulations while maintaining readiness for inspections and audits for artwork, packaging, and distribution operations.</li>\n\n</ul></ul></ul></ul></ul></ul></div>"},{"text":"Candidate Requirements:","content":"<div>\n\n<li style=\"list-style: none;\">\n\n</li><li>A bachelor’s degree in supply chain management, chemistry, or a related field.</li>\n<li>Demonstrated experience in Biopharma industry, with a minimum of 10 years at Associate Director level or above.</li>\n<li>Experience in start-up/ rare disease products is a plus.</li>\n<li>Commercial product launch experience including artwork, packaging operations and transportation/distribution.</li>\n<li>Strong strategic planning skills with a strong interest in developing team and individuals.</li>\n<li>Strong problem-solving abilities, attention to detail, and ability to make data-driven decisions.</li>\n<li>Excellent verbal and written communication skills, with the ability to interact with internal teams, external partners, and regulatory bodies.</li>\n<li>Strong organizational skills with the ability to manage multiple projects and deadlines effectively.</li>\n<li>Good level of spoken and written English.</li>\n\n\n\n</div>"}],"text":"Director, Supply Chain Japan","country":"JP","workplaceType":"hybrid","opening":"<div><em>Scholar Rock is a late-stage <span data-ogsc=\"red\">global&nbsp;</span>biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity.&nbsp;Scholar Rock&nbsp;works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at </em><a class=\"postings-link\" href=\"http://www.scholarrock.com/\" target=\"_blank\" rel=\"noopener noreferrer\"><em>ScholarRock.com</em></a><em> and follow </em><a class=\"postings-link\" href=\"http://www.twitter.com/scholarrock\" target=\"_blank\" rel=\"noopener noreferrer\"><em>@ScholarRock</em></a><em> on X and on&nbsp;</em><a class=\"postings-link\" href=\"https://www.linkedin.com/company/scholar-rock\" target=\"_blank\" rel=\"noopener noreferrer\"><em>LinkedIn</em></a><em>.</em></div>\n<div>&nbsp;</div>\n<div><strong style=\"font-size: 18px;\">Summary of Position:</strong></div>","openingPlain":"Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at ScholarRock.com and follow @ScholarRock on X and on LinkedIn.\n \nSummary of Position:\n","descriptionBody":"<div>\n<p style=\"text-align: justify; margin: 0in; font-size: 12pt; font-family: Cambria, serif;\"><span style=\"font-size: 10.0pt; font-family: Arial, sans-serif;\">The Director of Supply Chain is responsible for building, implementing, and managing the commercial supply chain for Scholar Rock in Japan. The role will oversee daily operations relating to artwork, secondary packaging and distribution activities and will work closely with Scholar Rock colleagues globally, primarily in the US and Ireland. </span><span style=\"font-size: 10.0pt; font-family: Arial, sans-serif;\">The position requires strong leadership, problem-solving, and analytical skills to optimize operational efficiency, reduce costs, and ensure products are reliably and compliantly supplied across Japan.</span></p>\n</div>","descriptionBodyPlain":"The Director of Supply Chain is responsible for building, implementing, and managing the commercial supply chain for Scholar Rock in Japan. The role will oversee daily operations relating to artwork, secondary packaging and distribution activities and will work closely with Scholar Rock colleagues globally, primarily in the US and Ireland. The position requires strong leadership, problem-solving, and analytical skills to optimize operational efficiency, reduce costs, and ensure products are reliably and compliantly supplied across Japan.\n","hostedUrl":"https://jobs.lever.co/scholarrock/279d2e8f-5901-4819-911d-0a64b720ed90","applyUrl":"https://jobs.lever.co/scholarrock/279d2e8f-5901-4819-911d-0a64b720ed90/apply"},{"additionalPlain":"Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. \n","additional":"<div><em>Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees</em>.&nbsp;</div>","categories":{"commitment":"Full-Time","department":"Development","location":"Cambridge, MA","team":"Clinical Pharmacology","allLocations":["Cambridge, MA"]},"createdAt":1785857897967,"descriptionPlain":"Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at ScholarRock.com and follow @ScholarRock on X and on LinkedIn.\n \nSummary of Position:\n","description":"<div><em>Scholar Rock is a late-stage <span data-ogsc=\"red\">global&nbsp;</span>biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity.&nbsp;Scholar Rock&nbsp;works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at </em><a rel=\"noopener noreferrer\" href=\"http://www.scholarrock.com/\" class=\"postings-link\"><em>ScholarRock.com</em></a><em> and follow </em><a rel=\"noopener noreferrer\" href=\"http://www.twitter.com/scholarrock\" class=\"postings-link\"><em>@ScholarRock</em></a><em> on X and on&nbsp;</em><a rel=\"noopener noreferrer\" href=\"https://www.linkedin.com/company/scholar-rock\" class=\"postings-link\"><em>LinkedIn</em></a><em>.</em></div>\n<div>&nbsp;</div>\n<div><strong style=\"font-size: 18px;\">Summary of Position:</strong></div><div><br></div><div>Scholar Rock is seeking a motivated, energetic, and outstanding individual with experience in clinical pharmacology and pharmacometrics to join our team in developing novel biologic therapies that target protein growth factors in the disease microenvironment. The Director/Senior Director of Clinical Pharmacology, reporting to the Head of Clinical Pharmacology, will have strong quantitative clinical pharmacology skills and hands-on modeling and simulation experience. This individual will be responsible for the analysis and interpretation of PK, PD, and efficacy data to guide the development of biologics including monoclonal antibodies.&nbsp;</div>","id":"15589660-d6ca-4b61-acc8-2a31e26aa4ed","lists":[{"text":"Position Responsibilities","content":"\n<li>Lead clinical pharmacology strategies across multiple programs at various stages of clinical development</li>\n<li>Execute modeling and simulation plans including PK/PD, population PK, and exposure-response analyses to guide clinical trial design, dose selection and optimization</li>\n<li>Develop IV to SC transition dosing plans</li>\n<li>Provide pediatric clinical pharmacology expertise and co-lead workstreams related to formulation development and sub-cutaneous route of administration &nbsp;</li>\n<li>Apply model-based drug development principles to answer key development questions enabling efficient drug development</li>\n<li>Contribute to preparation of regulatory documents and participate in discussions with Regulatory Agencies, with a focus on&nbsp;Model-informed Drug Development (MIDD).</li>\n<li>Contribute to clinical protocol design, study execution, data analysis, and writing clinical study reports</li>\n<li>Collaborate and mentor bioanalytical and translational team to develop comprehensive preclinical and clinical PK/PD strategy</li>\n"},{"text":"Candidate Requirements","content":"\n<li>PhD in pharmacokinetics or pharmacology</li>\n<li>7-10 years of experience in pharma/biotech industry, with proven track record of using clinical pharmacology to guide clinical trial/dosing decision</li>\n<li>Strong background in quantitative drug development and a desire to work collaboratively across different functional areas, as well as with external vendors and partners</li>\n<li>Experience in modeling and simulation of pharmacokinetic, pharmacodynamic, and exposure-response analyses, including expertise with population modeling</li>\n<li>Ability to interpret and integrate complex data sets across multiple disciplines including pharmacology, DMPK, toxicology assessing the clinical relevance</li>\n<li>Strong interpersonal writing and presentation skills, as well as the ability to function in a team environment are essential</li>\n<li>Understands the drug development process from pre-IND through BLA</li>\n<li>Highly organized, outcome-oriented, self-motivated performer</li>\n"}],"salaryRange":{"min":225000,"max":315000,"currency":"USD","interval":"per-year-salary"},"text":"Director/Sr. Director, Clinical Pharmacology","country":"US","workplaceType":"onsite","opening":"<div><em>Scholar Rock is a late-stage <span data-ogsc=\"red\">global&nbsp;</span>biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity.&nbsp;Scholar Rock&nbsp;works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at </em><a class=\"postings-link\" href=\"http://www.scholarrock.com/\" target=\"_blank\" rel=\"noopener noreferrer\"><em>ScholarRock.com</em></a><em> and follow </em><a class=\"postings-link\" href=\"http://www.twitter.com/scholarrock\" target=\"_blank\" rel=\"noopener noreferrer\"><em>@ScholarRock</em></a><em> on X and on&nbsp;</em><a class=\"postings-link\" href=\"https://www.linkedin.com/company/scholar-rock\" target=\"_blank\" rel=\"noopener noreferrer\"><em>LinkedIn</em></a><em>.</em></div>\n<div>&nbsp;</div>\n<div><strong style=\"font-size: 18px;\">Summary of Position:</strong></div>","openingPlain":"Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at ScholarRock.com and follow @ScholarRock on X and on LinkedIn.\n \nSummary of Position:\n","descriptionBody":"<div>Scholar Rock is seeking a motivated, energetic, and outstanding individual with experience in clinical pharmacology and pharmacometrics to join our team in developing novel biologic therapies that target protein growth factors in the disease microenvironment. The Director/Senior Director of Clinical Pharmacology, reporting to the Head of Clinical Pharmacology, will have strong quantitative clinical pharmacology skills and hands-on modeling and simulation experience. This individual will be responsible for the analysis and interpretation of PK, PD, and efficacy data to guide the development of biologics including monoclonal antibodies.&nbsp;</div>","descriptionBodyPlain":"","hostedUrl":"https://jobs.lever.co/scholarrock/15589660-d6ca-4b61-acc8-2a31e26aa4ed","applyUrl":"https://jobs.lever.co/scholarrock/15589660-d6ca-4b61-acc8-2a31e26aa4ed/apply"},{"additionalPlain":"Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. \n","additional":"<div><em>Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees</em>.&nbsp;</div>","categories":{"commitment":"Full-Time - Remote","department":"Commercial","location":"Cambridge, MA","team":"Commercial Operations","allLocations":["Cambridge, MA"]},"createdAt":1785264844227,"descriptionPlain":"Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at ScholarRock.com and follow @ScholarRock on X and on LinkedIn.\n \nSummary of Position:\n\n\nThe Regional Director, Rx Onboarding and Care Coordination, East is a field-based regional leader responsible for leading, coaching, and developing a team of Rx Onboarding and Care Coordinators (ROCC) who support patients and caregivers throughout their SMA treatment journey.\nThis role serves as part of the Access, Case Management and Education Center of Excellence (ACE CoE) driving consistent execution, role clarity, governance, best practices, and escalation management across the East Region. The ROCC Lead partners closely with cross-functional stakeholders to improve patient onboarding, treatment initiation, access, and ongoing therapy support while ensuring a consistent patient, caregiver, healthcare provider, and infusion center experience.\nThe ideal candidate brings strong people leadership, patient access expertise, rare disease experience, and the ability to drive execution in a dynamic launch environment.\n","description":"<div><em>Scholar Rock is a late-stage <span data-ogsc=\"red\">global&nbsp;</span>biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity.&nbsp;Scholar Rock&nbsp;works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at </em><a rel=\"noopener noreferrer\" href=\"http://www.scholarrock.com/\" class=\"postings-link\"><em>ScholarRock.com</em></a><em> and follow </em><a rel=\"noopener noreferrer\" href=\"http://www.twitter.com/scholarrock\" class=\"postings-link\"><em>@ScholarRock</em></a><em> on X and on&nbsp;</em><a rel=\"noopener noreferrer\" href=\"https://www.linkedin.com/company/scholar-rock\" class=\"postings-link\"><em>LinkedIn</em></a><em>.</em></div>\n<div>&nbsp;</div>\n<div><strong style=\"font-size: 18px;\">Summary of Position:</strong></div><div><br></div><div>\n<p>The <strong>Regional Director, Rx Onboarding and Care Coordination, East</strong> is a field-based regional leader responsible for leading, coaching, and developing a team of Rx Onboarding and Care Coordinators (ROCC) who support patients and caregivers throughout their SMA treatment journey.</p>\n<p>This role serves as part of the&nbsp;<strong>Access, Case Management and Education Center of Excellence (ACE CoE)</strong> driving consistent execution, role clarity, governance, best practices, and escalation management across the East Region. The ROCC Lead partners closely with cross-functional stakeholders to improve patient onboarding, treatment initiation, access, and ongoing therapy support while ensuring a consistent patient, caregiver, healthcare provider, and infusion center experience.</p>\n<p>The ideal candidate brings strong people leadership, patient access expertise, rare disease experience, and the ability to drive execution in a dynamic launch environment.</p>\n</div>","id":"99842c07-a738-4f06-9cc7-bd8af5a1cfc5","lists":[{"text":"Position Responsibilities: ","content":"<div>\n<h3>Team Leadership &amp; Development</h3>\n\n<li>Lead, coach, and develop a team of ROCCs across the East Region by providing ongoing performance feedback, field coaching, and development support.</li>\n<li>Reinforce role clarity, compliant ways of working, and patient-centric behaviors.</li>\n<li>Support onboarding, training, and capability development across the team.</li>\n<li>Foster a culture of accountability, collaboration, empathy, and continuous improvement.</li>\n\n<h3>Center of Excellence Leadership</h3>\n\n<li>Serve as regional lead for the ROCC role within the ACE CoE.</li>\n<li>Establish and reinforce standards, best practices, and operating procedures.</li>\n<li>Ensure consistent execution, governance, and accountability across patient support activities.</li>\n<li>Lead regional escalation management and support resolution of complex access, reimbursement, site-of-care, and patient experience challenges.</li>\n<li>Identify operational gaps, emerging trends, and patient journey barriers and partner cross-functionally to implement solutions.</li>\n<li>Share field insights to inform CoE standards, training, metrics, and process improvements.</li>\n\n<h3>Patient Access &amp; Care Coordination</h3>\n\n<li>Oversee patient onboarding, education, access coordination, and care navigation activities throughout the treatment journey.</li>\n<li>Support complex patient cases and provide guidance on non-clinical barriers to treatment.</li>\n<li>Help ensure patients and caregivers have access to appropriate educational, financial, and logistical support resources.</li>\n<li>Monitor patient journey metrics and identify opportunities to improve treatment initiation and ongoing patient experience.</li>\n\n<h3>Cross-Functional Leadership</h3>\n\n<li>Partner closely with Field Reimbursement, Infusion Educators, Case Managers, Account Managers, Specialty Pharmacy, Advocacy, Marketing, Compliance, and other internal stakeholders.</li>\n<li>Drive collaboration to resolve barriers, improve processes, and deliver a seamless patient and provider experience.</li>\n<li>Communicate regional insights, risks, trends, and recommendations to leadership.</li>\n\n<h3>Operational Excellence &amp; Compliance</h3>\n\n<li>Establish consistent operating rhythms, team communications, case reviews, and coaching activities.</li>\n<li>Monitor execution, documentation quality, and follow-up on patient support activities.</li>\n<li>Ensure compliance with all company policies and applicable legal, regulatory, privacy, and reporting requirements.</li>\n<li>Support effective use of systems, data, reporting, and escalation processes to drive execution excellence.</li>\n\n</div>"},{"text":"Candidate Requirements:","content":"<div>\n\n<li style=\"list-style-type: revert;\">Bachelor’s degree required; advanced degree preferred.</li>\n<li>8+ years of experience in biotechnology, pharmaceuticals, patient services, patient access, reimbursement, HUB services, case management, field reimbursement, or related functions.</li>\n<li>Prior experience leading patient support, access, reimbursement, care coordination, or field-based teams.</li>\n<li>Strong knowledge of patient access, benefit verification, prior authorization, affordability programs, specialty pharmacy, HUB services, and reimbursement processes.</li>\n<li>Experience supporting complex therapies, rare diseases, infusion therapy, buy-and-bill, and site-of-care models preferred.</li>\n<li>Demonstrated success leading teams, managing escalations, and driving consistent execution across regions.</li>\n<li>Strong cross-functional collaboration, communication, and leadership skills.</li>\n<li>Launch experience preferred.</li>\n<li>Knowledge of HIPAA, FDA, OIG, adverse event reporting, and compliance standards.</li>\n<li>Bilingual Spanish preferred.</li>\n\n</div>"}],"salaryRange":{"min":215000,"max":250000,"currency":"USD","interval":"per-year-salary"},"text":"Regional Director, Rx Onboarding and Care Coordination, East","country":"US","workplaceType":"remote","opening":"<div><em>Scholar Rock is a late-stage <span data-ogsc=\"red\">global&nbsp;</span>biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity.&nbsp;Scholar Rock&nbsp;works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at </em><a class=\"postings-link\" href=\"http://www.scholarrock.com/\" target=\"_blank\" rel=\"noopener noreferrer\"><em>ScholarRock.com</em></a><em> and follow </em><a class=\"postings-link\" href=\"http://www.twitter.com/scholarrock\" target=\"_blank\" rel=\"noopener noreferrer\"><em>@ScholarRock</em></a><em> on X and on&nbsp;</em><a class=\"postings-link\" href=\"https://www.linkedin.com/company/scholar-rock\" target=\"_blank\" rel=\"noopener noreferrer\"><em>LinkedIn</em></a><em>.</em></div>\n<div>&nbsp;</div>\n<div><strong style=\"font-size: 18px;\">Summary of Position:</strong></div>","openingPlain":"Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at ScholarRock.com and follow @ScholarRock on X and on LinkedIn.\n \nSummary of Position:\n","descriptionBody":"<div>\n<p>The <strong>Regional Director, Rx Onboarding and Care Coordination, East</strong> is a field-based regional leader responsible for leading, coaching, and developing a team of Rx Onboarding and Care Coordinators (ROCC) who support patients and caregivers throughout their SMA treatment journey.</p>\n<p>This role serves as part of the&nbsp;<strong>Access, Case Management and Education Center of Excellence (ACE CoE)</strong> driving consistent execution, role clarity, governance, best practices, and escalation management across the East Region. The ROCC Lead partners closely with cross-functional stakeholders to improve patient onboarding, treatment initiation, access, and ongoing therapy support while ensuring a consistent patient, caregiver, healthcare provider, and infusion center experience.</p>\n<p>The ideal candidate brings strong people leadership, patient access expertise, rare disease experience, and the ability to drive execution in a dynamic launch environment.</p>\n</div>","descriptionBodyPlain":"The Regional Director, Rx Onboarding and Care Coordination, East is a field-based regional leader responsible for leading, coaching, and developing a team of Rx Onboarding and Care Coordinators (ROCC) who support patients and caregivers throughout their SMA treatment journey.\nThis role serves as part of the Access, Case Management and Education Center of Excellence (ACE CoE) driving consistent execution, role clarity, governance, best practices, and escalation management across the East Region. The ROCC Lead partners closely with cross-functional stakeholders to improve patient onboarding, treatment initiation, access, and ongoing therapy support while ensuring a consistent patient, caregiver, healthcare provider, and infusion center experience.\nThe ideal candidate brings strong people leadership, patient access expertise, rare disease experience, and the ability to drive execution in a dynamic launch environment.\n","hostedUrl":"https://jobs.lever.co/scholarrock/99842c07-a738-4f06-9cc7-bd8af5a1cfc5","applyUrl":"https://jobs.lever.co/scholarrock/99842c07-a738-4f06-9cc7-bd8af5a1cfc5/apply"},{"additionalPlain":"Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. \n","additional":"<div><em>Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees</em>.&nbsp;</div>","categories":{"commitment":"Full-Time","department":"G&A","location":"Cambridge, MA","team":"Finance","allLocations":["Cambridge, MA"]},"createdAt":1787065262868,"descriptionPlain":"Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at ScholarRock.com and follow @ScholarRock on X and on LinkedIn.\n \nSummary of Position:\n","description":"<div><em>Scholar Rock is a late-stage <span data-ogsc=\"red\">global&nbsp;</span>biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity.&nbsp;Scholar Rock&nbsp;works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at </em><a rel=\"noopener noreferrer\" href=\"http://www.scholarrock.com/\" class=\"postings-link\"><em>ScholarRock.com</em></a><em> and follow </em><a rel=\"noopener noreferrer\" href=\"http://www.twitter.com/scholarrock\" class=\"postings-link\"><em>@ScholarRock</em></a><em> on X and on&nbsp;</em><a rel=\"noopener noreferrer\" href=\"https://www.linkedin.com/company/scholar-rock\" class=\"postings-link\"><em>LinkedIn</em></a><em>.</em></div>\n<div>&nbsp;</div>\n<div><strong style=\"font-size: 18px;\">Summary of Position:</strong></div><div><br></div><div>The Senior Accountant will play an important role in supporting the monthly close process, maintaining accurate financial records, and helping ensure the Company’s accounting processes are timely, well controlled, and scalable as the business grows. This role will be responsible for preparing journal entries, account reconciliations, and supporting schedules across key areas such as cash, prepaid expenses and accruals, G&amp;A activity, fixed assets, and other general ledger accounts.</div>\n<div><br>The Senior Accountant will collaborate closely with members of the Accounting team to support internal reporting, external reporting, audit requests, SOX compliance, and process improvement initiatives. This position is a great opportunity for someone who is detail-oriented, organized, pro-active, and excited to gain exposure to a broad range of accounting areas within a growing public biotechnology company. The ideal candidate will be comfortable working in a fast-paced environment, able to manage multiple priorities, and willing to take initiative. This role requires strong Excel skills, clear communication, attention to detail, and a team-oriented approach.</div>","id":"17167a28-80ae-4126-a2c7-cb23b1bb06ec","lists":[{"text":"Position Responsibilities","content":"\n<li>Prepare month-end journal entries and account reconciliations/supporting schedules across cash, prepaid expenses, fixed assets, accruals, G&amp;A activity, and other GL accounts</li>\n<li>Perform account analyses, investigate variances, and support timely, accurate completion of monthly/quarterly close activities</li>\n<li>Prepare schedules and documentation supporting internal reporting, external reporting, audits, quarterly reviews, and SOX compliance</li>\n<li>Partner with cross-functional teams to gather information needed for accounting entries and analysis</li>\n<li>Support efforts to continuously drive cross-functional improvements, as well as create process documentation</li>\n<li>Execute special ad-hoc projects as requested to support the greater Finance team</li>\n"},{"text":"Candidate Requirements","content":"\n<li>Bachelor’s degree in Accounting, Finance, or related field</li>\n<li>3-5 years of relevant accounting experience</li>\n<li>CPA or equivalent is preferred</li>\n<li>Life sciences, biotechnology, or pharmaceutical industry experience preferred</li>\n<li>Public company experience preferred</li>\n<li>NetSuite and/or SAP experience preferred</li>\n<li>Experience with month-end close, journal entries, reconciliations, and account analysis</li>\n<li>Exposure to SOX controls and audit support preferred</li>\n<li>Strong organizational skills and ability to manage multiple priorities in a fast-paced environment</li>\n<li>Ability to work independently, take initiative, and follow through on open items</li>\n<li>Strong communication skills and ability to work effectively with team members and cross-functional partners</li>\n<li>Strong Excel and computer skills required</li>\n<li>Strong attention to detail and ability to produce accurate, well-supported work</li>\n<li>Curious, proactive, and motivated to learn and grow within a developing accounting organization</li>\n"}],"text":"Senior Accountant","country":"US","workplaceType":"hybrid","opening":"<div><em>Scholar Rock is a late-stage <span data-ogsc=\"red\">global&nbsp;</span>biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity.&nbsp;Scholar Rock&nbsp;works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at </em><a class=\"postings-link\" href=\"http://www.scholarrock.com/\" target=\"_blank\" rel=\"noopener noreferrer\"><em>ScholarRock.com</em></a><em> and follow </em><a class=\"postings-link\" href=\"http://www.twitter.com/scholarrock\" target=\"_blank\" rel=\"noopener noreferrer\"><em>@ScholarRock</em></a><em> on X and on&nbsp;</em><a class=\"postings-link\" href=\"https://www.linkedin.com/company/scholar-rock\" target=\"_blank\" rel=\"noopener noreferrer\"><em>LinkedIn</em></a><em>.</em></div>\n<div>&nbsp;</div>\n<div><strong style=\"font-size: 18px;\">Summary of Position:</strong></div>","openingPlain":"Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at ScholarRock.com and follow @ScholarRock on X and on LinkedIn.\n \nSummary of Position:\n","descriptionBody":"<div>The Senior Accountant will play an important role in supporting the monthly close process, maintaining accurate financial records, and helping ensure the Company&rsquo;s accounting processes are timely, well controlled, and scalable as the business grows. This role will be responsible for preparing journal entries, account reconciliations, and supporting schedules across key areas such as cash, prepaid expenses and accruals, G&amp;A activity, fixed assets, and other general ledger accounts.</div>\n<div><br>The Senior Accountant will collaborate closely with members of the Accounting team to support internal reporting, external reporting, audit requests, SOX compliance, and process improvement initiatives. This position is a great opportunity for someone who is detail-oriented, organized, pro-active, and excited to gain exposure to a broad range of accounting areas within a growing public biotechnology company. The ideal candidate will be comfortable working in a fast-paced environment, able to manage multiple priorities, and willing to take initiative. This role requires strong Excel skills, clear communication, attention to detail, and a team-oriented approach.</div>","descriptionBodyPlain":"","hostedUrl":"https://jobs.lever.co/scholarrock/17167a28-80ae-4126-a2c7-cb23b1bb06ec","applyUrl":"https://jobs.lever.co/scholarrock/17167a28-80ae-4126-a2c7-cb23b1bb06ec/apply"},{"additionalPlain":"Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. \n","additional":"<div><em>Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees</em>.&nbsp;</div>","categories":{"commitment":"Full-Time","department":"Commercial","location":"Cambridge, MA","team":"Commercial Operations","allLocations":["Cambridge, MA"]},"createdAt":1777062341670,"descriptionPlain":"Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at ScholarRock.com and follow @ScholarRock on X and on LinkedIn.\n \nSummary of Position:\n\n\nThe Senior Director, Business Analytics will provide strategic leadership for enterprise‑wide analytics supporting Scholar Rock’s commercial launch and long‑term growth. This role is responsible for defining the analytics vision and roadmap across commercial, ensuring data‑driven decision‑making at both the executive and operational levels.\nThe successful candidate will blend strong strategic thinking with hands‑on analytical leadership, deep cross‑functional collaboration, and experience operating in dynamic pre‑ and post‑launch environments. This is a high‑visibility role with direct impact on launch readiness, go‑to‑market execution, and performance management.\nIn addition, this role will identify critical business issues and growth opportunities, partner closely with cross‑functional teams, and embed an external market perspective into the company’s strategic direction.\n","description":"<div><em>Scholar Rock is a late-stage <span data-ogsc=\"red\">global&nbsp;</span>biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity.&nbsp;Scholar Rock&nbsp;works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at </em><a rel=\"noopener noreferrer\" href=\"http://www.scholarrock.com/\" class=\"postings-link\"><em>ScholarRock.com</em></a><em> and follow </em><a rel=\"noopener noreferrer\" href=\"http://www.twitter.com/scholarrock\" class=\"postings-link\"><em>@ScholarRock</em></a><em> on X and on&nbsp;</em><a rel=\"noopener noreferrer\" href=\"https://www.linkedin.com/company/scholar-rock\" class=\"postings-link\"><em>LinkedIn</em></a><em>.</em></div>\n<div>&nbsp;</div>\n<div><strong style=\"font-size: 18px;\">Summary of Position:</strong></div><div><br></div><div>\n<p>The Senior Director, Business Analytics will provide strategic leadership for enterprise‑wide analytics supporting Scholar Rock’s commercial launch and long‑term growth. This role is responsible for defining the analytics vision and roadmap across commercial, ensuring data‑driven decision‑making at both the executive and operational levels.</p>\n<p>The successful candidate will blend strong strategic thinking with hands‑on analytical leadership, deep cross‑functional collaboration, and experience operating in dynamic pre‑ and post‑launch environments. This is a high‑visibility role with direct impact on launch readiness, go‑to‑market execution, and performance management.</p>\n<p>In addition, this role will identify critical business issues and growth opportunities, partner closely with cross‑functional teams, and embed an external market perspective into the company’s strategic direction.</p>\n</div>","id":"104947d2-5e70-4ad9-8112-50f77aa10162","lists":[{"text":"Position Responsibilities:","content":"<div>\n<ul type=\"disc\">\n<li>Define and lead the enterprise analytics strategy aligned with Scholar Rock’s commercial and corporate objectives.</li>\n<li>Establish analytics as a strategic business partner across Commercial, Market Access, Medical, and related functions.</li>\n<li>Synthesize complex analyses into clear, compelling insights for senior leadership.</li>\n<li>Leads Analytics efforts to support QBRs/MBRs, launch reviews, and strategic planning discussions with data‑driven insights.</li>\n<li>Develop and own the analytics roadmap, balancing near‑term launch needs with scalable, long‑term capabilities.</li>\n<li>Provide insights to inform critical business decisions and identify potential drivers of revenue growth.</li>\n<li>Evolve and co‑manage the data infrastructure, including modernization of national‑level reporting and performance metrics.</li>\n<li>Serve as a primary point of contact for executive‑level insight and analytics requests.</li>\n<li>Build, lead, and manage a high‑performing analytics team, ensuring alignment on goals, timelines, and forecasting methodologies.</li>\n<li>Deliver actionable insights into HCP, HCO, and patient dynamics to support brand strategy and execution.</li>\n<li>Translate complex datasets into insights that inform patient‑centric decision making.</li>\n<li>Partner closely with the broader Commercial organization to understand key business questions and align analytics and operational strategies.</li>\n<li>Perform other responsibilities as assigned.</li>\n\n</ul></div>"},{"text":"Candidate Requirements:","content":"<div>\n\n<li>Bachelor’s degree in business, science or related field. A master’s degree (MBA) strongly preferred.</li>\n<li>10-15 years of experience working in the pharmaceutical or biotech industry with five plus years supporting field sales teams.</li>\n<li>Proven experience leading analytics in a pre‑launch or early‑launch environment.</li>\n<li>Strong understanding of commercial analytics, patient services, Medical and market access analytics.</li>\n<li>Demonstrated ability to influence senior stakeholders and operate effectively in a matrixed organization.</li>\n<li>Knowledge of Medicare, Medicaid, and private insurer reimbursement methodology and understanding of healthcare benefits (deductible, out of pocket, benefit exclusions, etc.)</li>\n<li>Familiarity with or exposure to both US and ex-US commercial requirements</li>\n<li>Experience working cross functionally with legal, compliance, R&amp;D, clinical and other partners</li>\n<li>Strong analytical skills with the capability to appropriately define issues, questions and data; to comprehend quantitative methods and analytical techniques; to perform accurate analysis (correctly calculated numbers, accurate graphs); to cross-check data and assumptions; to document and establish data trails; and to think creatively about different ways to analyze data and information</li>\n<li>Excellent quantitative background that supports the analysis of data to better understand market dynamics and provide insights into product performance and marketing strategy.</li>\n<li>Strong interpersonal skills with demonstrated ability to drive toward consensus</li>\n<li>Exceptional persuasive written and verbal communication skills. Willingness to present the facts and put forth hypothesis in the face of differing opinions</li>\n<li>Excellent presentation skills with the ability to establish logical flow and story and skilled in choosing best graphic representation for points to be made.&nbsp; Experienced presenting to senior management</li>\n<li>Ability to adjust to changing needs within the organization and flexibility to change priorities as needed</li>\n<li>Ability to self direct projects and work with little supervision.</li>\n<li>Demonstrated values-based skills and strong work ethic</li>\n<li>Pharmaceutical launch experience with an emphasis on building infrastructure and processes that do not currently exist</li>\n\n</div>"}],"salaryRange":{"min":250000,"max":325000,"currency":"USD","interval":"per-year-salary"},"text":"Senior Director, Business Analytics","country":"US","workplaceType":"hybrid","opening":"<div><em>Scholar Rock is a late-stage <span data-ogsc=\"red\">global&nbsp;</span>biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity.&nbsp;Scholar Rock&nbsp;works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at </em><a class=\"postings-link\" href=\"http://www.scholarrock.com/\" target=\"_blank\" rel=\"noopener noreferrer\"><em>ScholarRock.com</em></a><em> and follow </em><a class=\"postings-link\" href=\"http://www.twitter.com/scholarrock\" target=\"_blank\" rel=\"noopener noreferrer\"><em>@ScholarRock</em></a><em> on X and on&nbsp;</em><a class=\"postings-link\" href=\"https://www.linkedin.com/company/scholar-rock\" target=\"_blank\" rel=\"noopener noreferrer\"><em>LinkedIn</em></a><em>.</em></div>\n<div>&nbsp;</div>\n<div><strong style=\"font-size: 18px;\">Summary of Position:</strong></div>","openingPlain":"Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at ScholarRock.com and follow @ScholarRock on X and on LinkedIn.\n \nSummary of Position:\n","descriptionBody":"<div>\n<p>The Senior Director, Business Analytics will provide strategic leadership for enterprise‑wide analytics supporting Scholar Rock&rsquo;s commercial launch and long‑term growth. This role is responsible for defining the analytics vision and roadmap across commercial, ensuring data‑driven decision‑making at both the executive and operational levels.</p>\n<p>The successful candidate will blend strong strategic thinking with hands‑on analytical leadership, deep cross‑functional collaboration, and experience operating in dynamic pre‑ and post‑launch environments. This is a high‑visibility role with direct impact on launch readiness, go‑to‑market execution, and performance management.</p>\n<p>In addition, this role will identify critical business issues and growth opportunities, partner closely with cross‑functional teams, and embed an external market perspective into the company&rsquo;s strategic direction.</p>\n</div>","descriptionBodyPlain":"The Senior Director, Business Analytics will provide strategic leadership for enterprise‑wide analytics supporting Scholar Rock’s commercial launch and long‑term growth. This role is responsible for defining the analytics vision and roadmap across commercial, ensuring data‑driven decision‑making at both the executive and operational levels.\nThe successful candidate will blend strong strategic thinking with hands‑on analytical leadership, deep cross‑functional collaboration, and experience operating in dynamic pre‑ and post‑launch environments. This is a high‑visibility role with direct impact on launch readiness, go‑to‑market execution, and performance management.\nIn addition, this role will identify critical business issues and growth opportunities, partner closely with cross‑functional teams, and embed an external market perspective into the company’s strategic direction.\n","hostedUrl":"https://jobs.lever.co/scholarrock/104947d2-5e70-4ad9-8112-50f77aa10162","applyUrl":"https://jobs.lever.co/scholarrock/104947d2-5e70-4ad9-8112-50f77aa10162/apply"},{"additionalPlain":"Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. \n","additional":"<div><em>Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees</em>.&nbsp;</div>","categories":{"department":"G&A","location":"Cambridge, MA","team":"Information Technology","allLocations":["Cambridge, MA"]},"createdAt":1786470661127,"descriptionPlain":"Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at ScholarRock.com and follow @ScholarRock on X and on LinkedIn.\n \nSummary of Position:\n\n\nScholar Rock is seeking a Senior Director, Cybersecurity to serve as the company’s Chief Information Security Officer, responsible for building and scaling enterprise cybersecurity capabilities that protect the organization’s people, data, technology assets, intellectual property, and business operations.\n\nReporting to the CIO, this role defines and executes the cybersecurity strategy and roadmap in partnership with enterprise stakeholders across technology, Legal, Privacy, HR, Finance, Quality, and business functions.\n \nThe successful candidate combines strategic leadership with hands-on execution, with deep expertise across cybersecurity architecture, engineering, operations, governance, risk management, and compliance. This leader will build scalable, risk-based cybersecurity capabilities for a growing biotechnology company, balancing current operational needs with the maturity required to support commercial growth, regulatory readiness, and future organizational scale.\n \nThis role is ideal for a cybersecurity leader who has successfully led multiple cybersecurity functions and is ready to assume broader enterprise cybersecurity leadership responsibilities in a lean, high-growth biotechnology environment.\n \n \n \n \nPosition Responsibilities\n","description":"<div><em>Scholar Rock is a late-stage <span data-ogsc=\"red\">global&nbsp;</span>biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity.&nbsp;Scholar Rock&nbsp;works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at </em><a rel=\"noopener noreferrer\" href=\"http://www.scholarrock.com/\" class=\"postings-link\"><em>ScholarRock.com</em></a><em> and follow </em><a rel=\"noopener noreferrer\" href=\"http://www.twitter.com/scholarrock\" class=\"postings-link\"><em>@ScholarRock</em></a><em> on X and on&nbsp;</em><a rel=\"noopener noreferrer\" href=\"https://www.linkedin.com/company/scholar-rock\" class=\"postings-link\"><em>LinkedIn</em></a><em>.</em></div>\n<div>&nbsp;</div>\n<div><strong style=\"font-size: 18px;\">Summary of Position:</strong></div><div><br></div><div>Scholar Rock is seeking a Senior Director, Cybersecurity to serve as the company’s Chief Information Security Officer, responsible for building and scaling enterprise cybersecurity capabilities that protect the organization’s people, data, technology assets, intellectual property, and business operations.</div>\n<div><br>Reporting to the CIO, this role defines and executes the cybersecurity strategy and roadmap in partnership with enterprise stakeholders across technology, Legal, Privacy, HR, Finance, Quality, and business functions.</div>\n<div>&nbsp;</div>\n<div>The successful candidate combines strategic leadership with hands-on execution, with deep expertise across cybersecurity architecture, engineering, operations, governance, risk management, and compliance. This leader will build scalable, risk-based cybersecurity capabilities for a growing biotechnology company, balancing current operational needs with the maturity required to support commercial growth, regulatory readiness, and future organizational scale.</div>\n<div>&nbsp;</div>\n<div>This role is ideal for a cybersecurity leader who has successfully led multiple cybersecurity functions and is ready to assume broader enterprise cybersecurity leadership responsibilities in a lean, high-growth biotechnology environment.</div>\n<div>&nbsp;</div>\n<div>&nbsp;</div>\n<div>&nbsp;</div>\n<div>&nbsp;</div>\n<h3>Position Responsibilities</h3>","id":"358ddbc2-ad21-4b19-a77c-0ac0173dd59e","lists":[{"text":"Cybersecurity Strategy & Program Leadership","content":"\n<li>Define and execute the enterprise <strong>cybersecurity strategy, roadmap, priorities, and operating model</strong></li>\n<li>Establish cybersecurity governance, policies, standards, and control frameworks aligned with business objectives and organizational growth</li>\n<li>Prioritize cybersecurity maturity initiatives based on business risk, regulatory expectations, commercial growth, and organizational scale</li>\n<li>Drive continuous improvement of cybersecurity capabilities and maturity across the organization</li>\n<li>Serve as the primary cybersecurity advisor to the CIO, Board of Directors, and business leadership</li>\n<li>Translate cybersecurity risks and opportunities into clear, actionable business recommendations</li>\n"},{"text":"Security Architecture & Engineering","content":"\n<li>Own the <strong>cybersecurity target-state architecture</strong> and security technology roadmap</li>\n<li>Lead cybersecurity architecture and engineering across cloud, infrastructure, identity, endpoint, network, application, SaaS, and data environments</li>\n<li>Embed <strong>secure-by-design and risk-based security principles</strong> across enterprise initiatives and technology platforms</li>\n<li>Partner with technology teams to integrate security requirements into solution design, implementation, and operational support models</li>\n<li>Evaluate, select, and optimize cybersecurity technologies and services that support business and regulatory requirements</li>\n"},{"text":"Security Operations & Cyber Resilience","content":"\n<li>Own security operations capabilities, including vulnerability management, incident response, security monitoring, identity security, and cyber resilience</li>\n<li>Establish and mature detection, response, recovery, and continuous improvement capabilities</li>\n<li>Lead cybersecurity incident response activities, executive communications, and post-incident reviews</li>\n<li>Partner with technology teams and service providers to strengthen operational security capabilities and reduce enterprise risk</li>\n<li>Support business continuity, disaster recovery, and cyber resilience planning in partnership with IT and business stakeholders</li>\n"},{"text":"Governance, Risk & Compliance","content":"\n<li>Lead the enterprise <strong>cybersecurity governance, risk, and compliance program</strong></li>\n<li>Establish and maintain cybersecurity risk management processes, risk assessments, remediation plans, and risk reporting</li>\n<li>Support SOX IT General Controls, user access governance, change management controls, and third-party risk management activities</li>\n<li>Maintain alignment with the <strong>NIST Cybersecurity Framework</strong> and applicable regulatory requirements</li>\n<li>Develop meaningful cybersecurity metrics, KPIs, KRIs, and executive reporting</li>\n<li>Prepare cybersecurity risk, maturity, roadmap, and investment updates for senior leadership and audit committee discussions, as appropriate</li>\n"},{"text":"Data Protection & Privacy","content":"\n<li>Lead cybersecurity capabilities to protect <strong>sensitive company data, intellectual property, clinical data, regulated information, and business-critical records</strong></li>\n<li>Partner with <strong>Legal, Privacy, Quality, Data &amp; Analytics, and business stakeholders</strong> to support data governance, data classification, access controls, and security-related privacy requirements</li>\n<li>Strengthen data protection capabilities across cloud, SaaS, endpoint, collaboration, and enterprise application environments</li>\n<li>Support implementation of <strong>privacy-by-design and least privilege principles</strong> in alignment with regulatory and business requirements</li>\n<li>Partner with Legal and Privacy on security considerations related to data protection, privacy obligations, vendor risk, and evolving regulatory expectations</li>\n"},{"text":"Audit, Quality & Regulatory Readiness","content":"\n<li>Serve as the cybersecurity lead for internal audits, external audits, inspections, and cybersecurity assessments</li>\n<li>Partner with Privacy, Legal, Quality, and IT stakeholders to ensure cybersecurity controls support compliance obligations</li>\n<li>Ensure cybersecurity controls support <strong>GxP-regulated systems, Computer System Validation, and data integrity</strong></li>\n<li>Drive timely remediation of audit findings, observations, and control deficiencies</li>\n"},{"text":"Vendor & Managed Service Leadership","content":"\n<li>Define and lead the <strong>cybersecurity operating model</strong>, leveraging internal teams, managed service providers, consultants, and strategic partners</li>\n<li>Own strategic relationships with cybersecurity vendors, MSSPs, consultants, and external partners, including governance, performance management, and accountability</li>\n<li>Establish service expectations, SLAs, KPIs, KRIs, operational metrics, and accountability mechanisms for third-party providers</li>\n<li>Conduct operational and executive-level performance reviews to ensure cybersecurity services meet business, compliance, regulatory, and operational objectives</li>\n<li>Partner with Procurement, Legal, Finance, and IT leadership on vendor selection, contract negotiations, renewals, investment decisions, and build vs. buy vs. outsource decisions</li>\n"},{"text":"Executive Communication & Business Partnership","content":"\n<li>Develop and deliver cybersecurity strategy updates, risk assessments, roadmap reviews, audit results, and investment recommendations to senior leadership</li>\n<li>Communicate cybersecurity risks and opportunities in clear business, operational, regulatory, and financial terms</li>\n<li>Build trusted relationships across business and technology functions</li>\n<li>Influence enterprise decision-making through practical, risk-based recommendations and effective stakeholder management</li>\n<li>Serve as a pragmatic advisor who enables business growth while maintaining appropriate risk discipline</li>\n"},{"text":"People Leadership","content":"\n<li>Lead, coach, mentor, and develop cybersecurity personnel and security-focused resources</li>\n<li>Provide leadership across employees, contractors, consultants, and managed service providers</li>\n<li>Foster a culture of accountability, continuous improvement, collaboration, and operational excellence</li>\n<li>Help shape the future cybersecurity organization as the company continues to scale</li>\n<li>Build a security culture that is practical, business-aligned, and appropriate for a growing commercial biotechnology company</li>\n"},{"text":"Candidate Requirements ","content":"\n<li>Bachelor’s degree in Information Security, Computer Science, Engineering, Information Technology, or a related discipline</li>\n<li><strong>12+ years of progressive cybersecurity experience</strong> with increasing leadership responsibilities</li>\n<li>Demonstrated leadership experience spanning cybersecurity architecture, engineering, and operational security functions</li>\n<li>Experience building, implementing, or maturing enterprise cybersecurity programs and capabilities</li>\n<li>Experience leading cybersecurity initiatives within regulated environments</li>\n<li>Strong knowledge of the <strong>NIST Cybersecurity Framework</strong>, cybersecurity governance, risk management, and security control implementation</li>\n<li>Experience supporting audits, compliance programs, risk assessments, and remediation activities</li>\n<li>Experience with data protection, access governance, third-party risk, and security controls for cloud, SaaS, endpoint, and enterprise application environments</li>\n<li>Experience managing cybersecurity vendors, managed service providers, and outsourced security services</li>\n<li>Proven ability to communicate effectively with executive leadership and influence organizational decision-making</li>\n<li>Strong presentation, communication, and stakeholder management skills</li>\n<li><strong>CISSP certification required</strong></li>\n"},{"text":"Preferred Qualifications","content":"\n<li>Experience in <strong>biotechnology, pharmaceutical, life sciences, healthcare, or medical device industries</strong></li>\n<li>Experience supporting <strong>GxP-regulated systems, Computer System Validation, Quality Management Systems, and inspection readiness activities</strong></li>\n<li>Experience supporting <strong>SOX compliance and IT General Controls</strong></li>\n<li>Familiarity with cloud security, identity and access management, vulnerability management, data protection, cybersecurity operations, and cyber resilience programs</li>\n<li>Experience partnering with Legal and Privacy teams on data protection, privacy-by-design, data classification, access control, and vendor risk considerations</li>\n<li>Experience supporting commercial-stage companies through growth, scale, geographic expansion, or increasing regulatory complexity</li>\n<li>CISM, CRISC, CCSP, GIAC, CISA, or ISO 27001 certifications preferred</li>\n"}],"salaryRange":{"min":245000,"max":325000,"currency":"USD","interval":"per-year-salary"},"text":"Senior Director, Chief Information Security Officer","country":"US","workplaceType":"onsite","opening":"<div><em>Scholar Rock is a late-stage <span data-ogsc=\"red\">global&nbsp;</span>biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity.&nbsp;Scholar Rock&nbsp;works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at </em><a class=\"postings-link\" href=\"http://www.scholarrock.com/\" target=\"_blank\" rel=\"noopener noreferrer\"><em>ScholarRock.com</em></a><em> and follow </em><a class=\"postings-link\" href=\"http://www.twitter.com/scholarrock\" target=\"_blank\" rel=\"noopener noreferrer\"><em>@ScholarRock</em></a><em> on X and on&nbsp;</em><a class=\"postings-link\" href=\"https://www.linkedin.com/company/scholar-rock\" target=\"_blank\" rel=\"noopener noreferrer\"><em>LinkedIn</em></a><em>.</em></div>\n<div>&nbsp;</div>\n<div><strong style=\"font-size: 18px;\">Summary of Position:</strong></div>","openingPlain":"Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at ScholarRock.com and follow @ScholarRock on X and on LinkedIn.\n \nSummary of Position:\n","descriptionBody":"<div>Scholar Rock is seeking a Senior Director, Cybersecurity to serve as the company&rsquo;s Chief Information Security Officer, responsible for building and scaling enterprise cybersecurity capabilities that protect the organization&rsquo;s people, data, technology assets, intellectual property, and business operations.</div>\n<div><br>Reporting to the CIO, this role defines and executes the cybersecurity strategy and roadmap in partnership with enterprise stakeholders across technology, Legal, Privacy, HR, Finance, Quality, and business functions.</div>\n<div>&nbsp;</div>\n<div>The successful candidate combines strategic leadership with hands-on execution, with deep expertise across cybersecurity architecture, engineering, operations, governance, risk management, and compliance. This leader will build scalable, risk-based cybersecurity capabilities for a growing biotechnology company, balancing current operational needs with the maturity required to support commercial growth, regulatory readiness, and future organizational scale.</div>\n<div>&nbsp;</div>\n<div>This role is ideal for a cybersecurity leader who has successfully led multiple cybersecurity functions and is ready to assume broader enterprise cybersecurity leadership responsibilities in a lean, high-growth biotechnology environment.</div>\n<div>&nbsp;</div>\n<div>&nbsp;</div>\n<div>&nbsp;</div>\n<div>&nbsp;</div>\n<h3>Position Responsibilities</h3>","descriptionBodyPlain":"Scholar Rock is seeking a Senior Director, Cybersecurity to serve as the company’s Chief Information Security Officer, responsible for building and scaling enterprise cybersecurity capabilities that protect the organization’s people, data, technology assets, intellectual property, and business operations.\n\nReporting to the CIO, this role defines and executes the cybersecurity strategy and roadmap in partnership with enterprise stakeholders across technology, Legal, Privacy, HR, Finance, Quality, and business functions.\n \nThe successful candidate combines strategic leadership with hands-on execution, with deep expertise across cybersecurity architecture, engineering, operations, governance, risk management, and compliance. This leader will build scalable, risk-based cybersecurity capabilities for a growing biotechnology company, balancing current operational needs with the maturity required to support commercial growth, regulatory readiness, and future organizational scale.\n \nThis role is ideal for a cybersecurity leader who has successfully led multiple cybersecurity functions and is ready to assume broader enterprise cybersecurity leadership responsibilities in a lean, high-growth biotechnology environment.\n \n \n \n \nPosition Responsibilities\n","hostedUrl":"https://jobs.lever.co/scholarrock/358ddbc2-ad21-4b19-a77c-0ac0173dd59e","applyUrl":"https://jobs.lever.co/scholarrock/358ddbc2-ad21-4b19-a77c-0ac0173dd59e/apply"},{"additionalPlain":"Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. \n","additional":"<div><em>Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees</em>.&nbsp;</div>","categories":{"commitment":"Full-Time","department":"Commercial","location":"Cambridge, MA","team":"Marketing","allLocations":["Cambridge, MA"]},"createdAt":1786371652473,"descriptionPlain":"Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at ScholarRock.com and follow @ScholarRock on X and on LinkedIn.\n \nSummary of Position:\n","description":"<div><em>Scholar Rock is a late-stage <span data-ogsc=\"red\">global&nbsp;</span>biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity.&nbsp;Scholar Rock&nbsp;works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at </em><a rel=\"noopener noreferrer\" href=\"http://www.scholarrock.com/\" class=\"postings-link\"><em>ScholarRock.com</em></a><em> and follow </em><a rel=\"noopener noreferrer\" href=\"http://www.twitter.com/scholarrock\" class=\"postings-link\"><em>@ScholarRock</em></a><em> on X and on&nbsp;</em><a rel=\"noopener noreferrer\" href=\"https://www.linkedin.com/company/scholar-rock\" class=\"postings-link\"><em>LinkedIn</em></a><em>.</em></div>\n<div>&nbsp;</div>\n<div><strong style=\"font-size: 18px;\">Summary of Position:</strong></div><div><br></div><div>The Senior Manager / Associate Director, HCP Marketing (US) will play a key role in the execution of Scholar Rock’s first U.S. commercial launch. This role will work with the HCP Marketing team lead to execute the HCP marketing strategy and ensure tactical pull-through for apitegromab, the first and only muscle-targeted therapy for spinal muscular atrophy (SMA).</div>\n<div><br>This individual will support the U.S. HCP brand strategy through commercialization, ensuring clear differentiation, compelling scientific communication, and flawless execution across channels. The role will work closely cross-functional partners deliver an integrated experience for HCPs and ensure brand continuity across tactics.</div>\n<div><br>This is a high-impact, high-visibility role within a fast-growing organization and an opportunity to contribute to the commercial foundation of Scholar Rock’s first marketed product.</div>\n<div>&nbsp;</div>\n<div>&nbsp;</div>\n<div>&nbsp;</div>\n<div>\n<h3><strong>Position Responsibilities</strong></h3>\n</div>","id":"7c01fab2-3a60-4800-841c-5ee0f4a095fe","lists":[{"text":"U.S. HCP Execution","content":"\n<li>Support execution of the U.S. HCP brand strategy for apitegromab, grounded in deep understanding of the SMA landscape, unmet need, and clinical data.</li>\n<li>Translate strategy into high-quality, compliant HCP promotional tactics across personal and non-personal channels.</li>\n<li>Partner with field-based team members to ensure strong integration between HCP marketing and field execution.</li>\n<li>Collaborate with agency partners and vendors to deliver best-in-class creative and execution.</li>\n"},{"text":"Cross-Functional Leadership","content":"\n<li>Serve as a connector across the U.S. Commercial Team, collaborating with Medical Affairs, Market Access, Patient Services, Regulatory, Legal, and Compliance.</li>\n<li>Build strong relationships with cross-functional partners in order to ensure brand continuity across all HCP-facing materials and tactics.</li>\n"},{"text":"Candidate Qualifications","content":"\n<li>Bachelor’s degree required; advanced degree preferred.</li>\n<li>3+ years of experience in pharmaceutical or biotechnology marketing, with experience in U.S. HCP marketing or Medical Education preferred</li>\n<li>MLR (or equivalent) experience strongly preferred.</li>\n<li>Understanding and experience navigating compliant HCP messaging.</li>\n<li>Strong strategic mindset with hands-on execution capability.</li>\n<li>Experience working in matrixed, cross-functional teams in a fast-paced environment.</li>\n<li>Excellent communication, influence, and stakeholder-management skills.</li>\n<li>Experience in neurology, neuromuscular disease, or rare disease preferred.</li>\n<li>Willingness to travel as needed (anticipated up to ~30%).</li>\n"}],"salaryRange":{"min":155000,"max":225000,"currency":"USD","interval":"per-year-salary"},"text":"Senior Manager / Associate Director, HCP Marketing (US)","country":"US","workplaceType":"hybrid","opening":"<div><em>Scholar Rock is a late-stage <span data-ogsc=\"red\">global&nbsp;</span>biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity.&nbsp;Scholar Rock&nbsp;works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at </em><a class=\"postings-link\" href=\"http://www.scholarrock.com/\" target=\"_blank\" rel=\"noopener noreferrer\"><em>ScholarRock.com</em></a><em> and follow </em><a class=\"postings-link\" href=\"http://www.twitter.com/scholarrock\" target=\"_blank\" rel=\"noopener noreferrer\"><em>@ScholarRock</em></a><em> on X and on&nbsp;</em><a class=\"postings-link\" href=\"https://www.linkedin.com/company/scholar-rock\" target=\"_blank\" rel=\"noopener noreferrer\"><em>LinkedIn</em></a><em>.</em></div>\n<div>&nbsp;</div>\n<div><strong style=\"font-size: 18px;\">Summary of Position:</strong></div>","openingPlain":"Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at ScholarRock.com and follow @ScholarRock on X and on LinkedIn.\n \nSummary of Position:\n","descriptionBody":"<div>The Senior Manager / Associate Director, HCP Marketing (US) will play a key role in the execution of Scholar Rock&rsquo;s first U.S. commercial launch. This role will work with the HCP Marketing team lead to execute the HCP marketing strategy and ensure tactical pull-through for apitegromab, the first and only muscle-targeted therapy for spinal muscular atrophy (SMA).</div>\n<div><br>This individual will support the U.S. HCP brand strategy through commercialization, ensuring clear differentiation, compelling scientific communication, and flawless execution across channels. The role will work closely cross-functional partners deliver an integrated experience for HCPs and ensure brand continuity across tactics.</div>\n<div><br>This is a high-impact, high-visibility role within a fast-growing organization and an opportunity to contribute to the commercial foundation of Scholar Rock&rsquo;s first marketed product.</div>\n<div>&nbsp;</div>\n<div>&nbsp;</div>\n<div>&nbsp;</div>\n<div>\n<h3><strong>Position Responsibilities</strong></h3>\n</div>","descriptionBodyPlain":"","hostedUrl":"https://jobs.lever.co/scholarrock/7c01fab2-3a60-4800-841c-5ee0f4a095fe","applyUrl":"https://jobs.lever.co/scholarrock/7c01fab2-3a60-4800-841c-5ee0f4a095fe/apply"},{"additionalPlain":"Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. \n","additional":"<div><em>Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees</em>.&nbsp;</div>","categories":{"commitment":"Full-Time","department":"G&A","location":"Cambridge, MA","team":"Legal","allLocations":["Cambridge, MA"]},"createdAt":1787687904541,"descriptionPlain":"Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at ScholarRock.com and follow @ScholarRock on X and on LinkedIn.\n \nSummary of Position:\n","description":"<div><em>Scholar Rock is a late-stage <span data-ogsc=\"red\">global&nbsp;</span>biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity.&nbsp;Scholar Rock&nbsp;works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at </em><a rel=\"noopener noreferrer\" href=\"http://www.scholarrock.com/\" class=\"postings-link\"><em>ScholarRock.com</em></a><em> and follow </em><a rel=\"noopener noreferrer\" href=\"http://www.twitter.com/scholarrock\" class=\"postings-link\"><em>@ScholarRock</em></a><em> on X and on&nbsp;</em><a rel=\"noopener noreferrer\" href=\"https://www.linkedin.com/company/scholar-rock\" class=\"postings-link\"><em>LinkedIn</em></a><em>.</em></div>\n<div>&nbsp;</div>\n<div><strong style=\"font-size: 18px;\">Summary of Position:</strong></div><div><br></div><div>\n<p>We are seeking a Senior Manager, Contracts to support our contracts processes and negotiations and provide general contracting advice across functional teams, including Development, Research, Commercial, and G&amp;A functions.&nbsp; This is an outstanding opportunity to join the legal team of a well-funded, growing biotechnology company preparing for its first product commercial launch.&nbsp; The primary responsibilities for this role will be drafting, revising, and negotiating a high volume of time-sensitive agreements.&nbsp; You will also have opportunities to implement special projects as needed, such as improvements to the contracts management system, managing external law firms, and creating and implementing new processes, trainings, reports, and systems related to managing the company’s agreements.&nbsp; You will be an integral member of a growing legal team where you will have the opportunity to be part of a collaborative team and work with experienced corporate and IP attorneys and compliance experts.&nbsp; This position reports to the Contracts Director and is located in the Cambridge office.&nbsp; Scholar Rock has flexibility with hybrid work arrangements.</p>\n</div>","id":"f531af82-63c3-43d2-ac06-3c2adb6a2398","lists":[{"text":"Position Responsibilities: ","content":"<div>\n\n<li>Lead the drafting and negotiations of contracts customary to a biotech company in the process of launching its first product, with a primary focus on Development, Research, Marketing, Regulatory, Quality, and G&amp;A contracts. Responsible for drafting and negotiating biotechnology-related agreements, including master service agreements, material transfer agreements, consulting agreements, confidentiality agreements, research agreements and clinical trial site agreements and related statements of work.</li>\n<li>Support and maintain contracts management system and associated contracting processes, including providing company-wide training, as needed.</li>\n<li>Provide legal contracts support across the organization, including quickly and effectively identifying complex legal and compliance issues and providing advice in a manner that integrates legal risk management with the company’s business objectives.&nbsp;</li>\n<li>Ability to work in a fast-paced environment, prioritize tasks, and successfully manage multiple projects.</li>\n<li>Develop and maintain strong business relationships across the company and contribute to cross-functional or departmental projects and teams.</li>\n<li>Maintain a positive team culture.</li>\n<li>Manage and complete any additional projects, as needed, including general corporate matters.</li>\n\n</div>"},{"text":"Candidate Requirements:","content":"<div>\n\n<li>5 or more years’ experience drafting and negotiating biotechnology-related agreements, including master service agreements, SOWs, research agreements, clinical trial related agreements, manufacturing or supply chain agreements, and commercial contracts in the life sciences industry</li>\n<li>Ability to work independently with strong attention to detail, sound judgment, organization and time management required</li>\n<li>Strong interpersonal skills and desire to engage collaboratively required</li>\n<li>Strong oral and written communication skills required, including the ability to provide concise and timely advice to business partners</li>\n<li>Familiarity with contracts management systems such as Ironclad and DocuSign eSignature preferred</li>\n<li>Bachelor’s degree from accredited university required</li>\n<li>Previous experience working on an in-house legal team at a biotechnology company preferred</li>\n\n</div>"}],"salaryRange":{"min":155000,"max":205000,"currency":"USD","interval":"per-year-salary"},"text":"Senior Manager, Contracts","country":"US","workplaceType":"hybrid","opening":"<div><em>Scholar Rock is a late-stage <span data-ogsc=\"red\">global&nbsp;</span>biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity.&nbsp;Scholar Rock&nbsp;works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at </em><a class=\"postings-link\" href=\"http://www.scholarrock.com/\" target=\"_blank\" rel=\"noopener noreferrer\"><em>ScholarRock.com</em></a><em> and follow </em><a class=\"postings-link\" href=\"http://www.twitter.com/scholarrock\" target=\"_blank\" rel=\"noopener noreferrer\"><em>@ScholarRock</em></a><em> on X and on&nbsp;</em><a class=\"postings-link\" href=\"https://www.linkedin.com/company/scholar-rock\" target=\"_blank\" rel=\"noopener noreferrer\"><em>LinkedIn</em></a><em>.</em></div>\n<div>&nbsp;</div>\n<div><strong style=\"font-size: 18px;\">Summary of Position:</strong></div>","openingPlain":"Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at ScholarRock.com and follow @ScholarRock on X and on LinkedIn.\n \nSummary of Position:\n","descriptionBody":"<div>\n<p>We are seeking a Senior Manager, Contracts to support our contracts processes and negotiations and provide general contracting advice across functional teams, including Development, Research, Commercial, and G&amp;A functions.&nbsp; This is an outstanding opportunity to join the legal team of a well-funded, growing biotechnology company preparing for its first product commercial launch.&nbsp; The primary responsibilities for this role will be drafting, revising, and negotiating a high volume of time-sensitive agreements.&nbsp; You will also have opportunities to implement special projects as needed, such as improvements to the contracts management system, managing external law firms, and creating and implementing new processes, trainings, reports, and systems related to managing the company&rsquo;s agreements.&nbsp; You will be an integral member of a growing legal team where you will have the opportunity to be part of a collaborative team and work with experienced corporate and IP attorneys and compliance experts.&nbsp; This position reports to the Contracts Director and is located in the Cambridge office.&nbsp; Scholar Rock has flexibility with hybrid work arrangements.</p>\n</div>","descriptionBodyPlain":"","hostedUrl":"https://jobs.lever.co/scholarrock/f531af82-63c3-43d2-ac06-3c2adb6a2398","applyUrl":"https://jobs.lever.co/scholarrock/f531af82-63c3-43d2-ac06-3c2adb6a2398/apply"},{"additionalPlain":"Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. \n","additional":"<div><em>Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees</em>.&nbsp;</div>","categories":{"commitment":"Full-Time","department":"G&A","location":"Cambridge, MA","team":"Information Technology","allLocations":["Cambridge, MA"]},"createdAt":1786471628055,"descriptionPlain":"Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at ScholarRock.com and follow @ScholarRock on X and on LinkedIn.\n \nSummary of Position:\n\n\nThe Senior Manager, Veeva Commercial & Data serves as the technology lead for enterprise applications and data supporting Scholar Rock’s Commercial and Medical organizations. Scholar Rock is establishing the application and data foundation required to support commercial launch, customer engagement, content management, medical communications, and future business growth, with Veeva serving as a core strategic platform.\nReporting to the Senior Director, Commercial & Data, the Senior Manager partners closely with Commercial, Medical Affairs, Commercial Operations, Regulatory, Legal, Compliance, Cybersecurity, Data & Analytics, Infrastructure & Cloud, and external technology partners to translate business priorities into scalable, secure, compliant, and sustainable technology solutions.\nThe role combines strong technical expertise with application ownership and delivery leadership. The Senior Manager leads solution delivery from requirements and design through implementation and ongoing support, maintains sufficient hands-on expertise to independently assess, configure, and troubleshoot complex Veeva solutions, and ensures internal and external delivery teams provide reliable, high-quality services.\nThe successful candidate will be comfortable moving between business conversations and technical decisions, understanding stakeholder priorities, shaping solutions, managing delivery and operational outcomes, and engaging directly with the technology when deeper expertise is required.\n \n \nPosition Responsibilities:\n","description":"<div><em>Scholar Rock is a late-stage <span data-ogsc=\"red\">global&nbsp;</span>biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity.&nbsp;Scholar Rock&nbsp;works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at </em><a rel=\"noopener noreferrer\" href=\"http://www.scholarrock.com/\" class=\"postings-link\"><em>ScholarRock.com</em></a><em> and follow </em><a rel=\"noopener noreferrer\" href=\"http://www.twitter.com/scholarrock\" class=\"postings-link\"><em>@ScholarRock</em></a><em> on X and on&nbsp;</em><a rel=\"noopener noreferrer\" href=\"https://www.linkedin.com/company/scholar-rock\" class=\"postings-link\"><em>LinkedIn</em></a><em>.</em></div>\n<div>&nbsp;</div>\n<div><strong style=\"font-size: 18px;\">Summary of Position:</strong></div><div><br></div><div>\n<p>The <strong>Senior Manager, Veeva Commercial &amp; Data</strong> serves as the technology lead for enterprise applications and data supporting Scholar Rock’s Commercial and Medical organizations. Scholar Rock is establishing the application and data foundation required to support commercial launch, customer engagement, content management, medical communications, and future business growth, with Veeva serving as a core strategic platform.</p>\n<p>Reporting to the Senior Director, Commercial &amp; Data, the Senior Manager partners closely with Commercial, Medical Affairs, Commercial Operations, Regulatory, Legal, Compliance, Cybersecurity, Data &amp; Analytics, Infrastructure &amp; Cloud, and external technology partners to translate business priorities into scalable, secure, compliant, and sustainable technology solutions.</p>\n<p>The role combines strong technical expertise with application ownership and delivery leadership. The Senior Manager leads solution delivery from requirements and design through implementation and ongoing support, maintains sufficient hands-on expertise to independently assess, configure, and troubleshoot complex Veeva solutions, and ensures internal and external delivery teams provide reliable, high-quality services.</p>\n<p>The successful candidate will be comfortable moving between business conversations and technical decisions, understanding stakeholder priorities, shaping solutions, managing delivery and operational outcomes, and engaging directly with the technology when deeper expertise is required.</p>\n<p>&nbsp;</p>\n<p>&nbsp;</p>\n<h3>Position Responsibilities:</h3>\n</div>","id":"3943729b-ad49-4a26-aa88-be59e2dac0e5","lists":[{"text":"Business Partnership & Solution Delivery","content":"\n<li>Serve as a trusted technology partner to Commercial, Medical Affairs, Commercial Operations, Regulatory, Legal, and Compliance stakeholders, developing a strong understanding of business priorities, processes, content workflows, launch needs, and evolving technology requirements.</li>\n<li>Translate business, operational, medical, promotional, and compliance requirements into solution options, technical requirements, delivery plans, and measurable outcomes.</li>\n<li>Partner with the Senior Manager, Veeva Regulatory and Data to execute the platform roadmap and align demand, priorities, dependencies, and delivery sequencing.</li>\n<li>Lead implementations, enhancements, integrations, releases, and continuous improvement initiatives across the Commercial and Medical application portfolio.</li>\n<li>Communicate solution recommendations, delivery status, risks, dependencies, and tradeoffs clearly to business and technology stakeholders.</li>\n<li>Partner with Commercial Operations, Medical Affairs, and business stakeholders to improve data quality, data stewardship, reporting enablement, and the effective use of commercial application data.</li>\n<li>Operate with a high degree of independence and judgment, making day-to-day application, technical, delivery, and operational decisions within established platform strategy and governance.</li>\n"},{"text":"Application & Technical Leadership","content":"\n<li>Provide technical leadership for Veeva CRM, PromoMats, MedComms, and related Commercial and Medical applications across solution design, configuration, integration, security, and lifecycle management.</li>\n<li>Design and configure complex Veeva solutions when needed and maintain the technical depth required to troubleshoot issues, assess alternatives, and independently validate partner recommendations.</li>\n<li>Establish scalable configuration, integration, security, and release practices that improve consistency, maintainability, and supportability.</li>\n<li>Lead technical design for integrations between Veeva and adjacent applications, data platforms, identity services, middleware, APIs, and other commercial or regulated technologies.</li>\n<li>Partner with Cybersecurity, Data &amp; Analytics, Infrastructure &amp; Cloud, Commercial Operations, Medical Affairs, Regulatory, Legal, and Compliance to ensure solutions align with enterprise standards, commercial compliance expectations, and regulatory requirements.</li>\n"},{"text":"Application Lifecycle & Operational Excellence","content":"\n<li>Own the day-to-day health, performance, supportability, and service quality of assigned Commercial and Medical applications.</li>\n<li>Ensure applications remain reliable, secure, compliant, scalable, and aligned with changing business requirements.</li>\n<li>Lead release planning, impact assessments, change execution, deployment readiness, user adoption support, and post-production support.</li>\n<li>Establish and monitor application health, service, delivery, quality, data quality, and adoption measures and use them to drive continuous improvement.</li>\n<li>Identify recurring issues, technical debt, lifecycle risks, data quality gaps, and service gaps and drive appropriate remediation.</li>\n<li>Ensure effective incident, problem, change, enhancement, and escalation management across applications within scope.</li>\n"},{"text":"Vendor & Delivery Management","content":"\n<li>Lead managed service providers, systems integrators, consultants, and other external partners supporting the Commercial and Medical application portfolio.</li>\n<li>Establish clear service, delivery, technical, and quality expectations and hold partners accountable for outcomes.</li>\n<li>Review and challenge vendor recommendations and technical solutions, ensuring decisions align with business requirements, architecture standards, commercial compliance expectations, and long-term application strategy.</li>\n<li>Manage delivery priorities, dependencies, escalations, risks, and performance across internal and external resources.</li>\n<li>Ensure effective documentation, knowledge transfer, operational readiness, and support transition for new and changed solutions.</li>\n<li>Build internal application knowledge and capability while using external partners strategically for capacity and specialized expertise.</li>\n"},{"text":"Commercial Compliance, MLR & Content Governance","content":"\n<li>Partner with Commercial, Medical Affairs, Regulatory, Legal, and Compliance on MLR, promotional review, medical review, content governance, and related system processes.</li>\n<li>Ensure solutions appropriately address applicable promotional, medical, privacy, security, content management, audit trail, access control, and compliance requirements.</li>\n<li>Support compliant content creation, review, approval, distribution, expiration, archival, reporting, and related operational processes.</li>\n<li>Support audits, compliance reviews, and risk assessments and coordinate technical response and remediation for application-related observations, findings, and corrective actions.</li>\n<li>Promote practical, risk-based compliance practices that support both business execution and sustainable technology delivery.</li>\n"},{"text":"Knowledge & Skills","content":"\n<li>Strong hands-on knowledge of Veeva CRM, PromoMats, MedComms, or related Veeva application architecture, configuration, integrations, security, and application lifecycle management.</li>\n<li>Strong understanding of enterprise application delivery, operations, support, and service management.</li>\n<li>Demonstrated ability to translate business requirements into practical technology solutions and successfully lead those solutions through implementation and operation.</li>\n<li>Experience managing vendor-delivered technology services and providing technical oversight to systems integrators and managed service providers.</li>\n<li>Strong working knowledge of commercial, medical, promotional, privacy, content governance, and compliance expectations as applied to technology.</li>\n<li>Ability to independently assess complex business and technical issues, make sound decisions, resolve ambiguity, and engage specialized expertise when appropriate.</li>\n<li>Strong stakeholder management, communication, prioritization, problem-solving, and decision-making skills.</li>\n<li>Ability to balance business priorities, technical sustainability, compliance requirements, operational risk, user adoption, and delivery commitments.</li>\n"},{"text":"Candidate Qualifications ","content":"\n<li style=\"list-style-type: none;\">\n<ul type=\"disc\">\n<li>Bachelor's degree or equivalent combination of education and relevant experience.</li>\n<li>8+ years of progressive experience in enterprise applications, technology delivery, application management, or related disciplines, preferably within pharmaceutical, biotechnology, or life sciences.</li>\n<li>4+ years of hands-on experience implementing, configuring, supporting, or delivering Veeva solutions across Commercial, Medical, promotional, content, or related business functions.</li>\n<li>Experience across Veeva applications supporting Commercial and Medical processes, such as CRM, PromoMats, MedComms, or related platforms.</li>\n<li>Experience leading implementations, enhancements, integrations, releases, and operational support for enterprise applications in compliance-driven environments.</li>\n<li>Experience managing technology delivery involving managed service providers, systems integrators, consultants, or vendor-delivered solutions.</li>\n<li>Experience serving as a platform owner, technical lead, solution delivery lead, or comparable technology leadership role supporting enterprise applications.</li>\n<li>Experience establishing trusted relationships with business stakeholders and translating complex business, commercial, medical, and compliance needs into technology outcomes.</li>\n<li>Demonstrated ability to independently assess complex business and technical issues, make sound decisions, resolve ambiguity, and drive solutions through implementation and ongoing operation.</li>\n<li>Working knowledge of pharmaceutical commercial, medical, promotional, privacy, and compliance requirements as applied to technology, including MLR, content governance, audit trails, access controls, and data privacy expectations.</li>\n<li>Veeva certification or advanced experience across one or more Commercial or Medical Veeva applications.</li>\n<li>Deep familiarity with the Veeva ecosystem, including CRM, Vault, Network, and related data integration patterns.</li>\n<li>Experience leading application delivery teams or platform teams.</li>\n<li>Experience supporting commercial data quality, data stewardship, reporting enablement, or data governance initiatives.</li>\n<li>Experience supporting commercial launch readiness within a biotechnology or pharmaceutical organization.</li>\n<li>Experience supporting commercial launch and global or multi-region operations.</li>\n<li>Experience standing up omnichannel engagement or next-best-action capabilities in a regulated pharmaceutical commercial environment.</li>\n<li>Familiarity with Patient Services, specialty pharmacy, hub operations, and associated commercial data flows.</li>\n<li>Prior experience in rare disease, specialty pharma, or biotechnology supporting Commercial or Medical operations.</li>\n<li>ITIL, Product Management, Agile, Project Management, or related certifications preferred.</li>\n\n\n</ul></li>"}],"salaryRange":{"min":155000,"max":195000,"currency":"USD","interval":"per-year-salary"},"text":"Senior Manager, Veeva Commercial & Data","country":"US","workplaceType":"onsite","opening":"<div><em>Scholar Rock is a late-stage <span data-ogsc=\"red\">global&nbsp;</span>biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity.&nbsp;Scholar Rock&nbsp;works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at </em><a class=\"postings-link\" href=\"http://www.scholarrock.com/\" target=\"_blank\" rel=\"noopener noreferrer\"><em>ScholarRock.com</em></a><em> and follow </em><a class=\"postings-link\" href=\"http://www.twitter.com/scholarrock\" target=\"_blank\" rel=\"noopener noreferrer\"><em>@ScholarRock</em></a><em> on X and on&nbsp;</em><a class=\"postings-link\" href=\"https://www.linkedin.com/company/scholar-rock\" target=\"_blank\" rel=\"noopener noreferrer\"><em>LinkedIn</em></a><em>.</em></div>\n<div>&nbsp;</div>\n<div><strong style=\"font-size: 18px;\">Summary of Position:</strong></div>","openingPlain":"Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at ScholarRock.com and follow @ScholarRock on X and on LinkedIn.\n \nSummary of Position:\n","descriptionBody":"<div>\n<p>The <strong>Senior Manager, Veeva Commercial &amp; Data</strong> serves as the technology lead for enterprise applications and data supporting Scholar Rock&rsquo;s Commercial and Medical organizations. Scholar Rock is establishing the application and data foundation required to support commercial launch, customer engagement, content management, medical communications, and future business growth, with Veeva serving as a core strategic platform.</p>\n<p>Reporting to the Senior Director, Commercial &amp; Data, the Senior Manager partners closely with Commercial, Medical Affairs, Commercial Operations, Regulatory, Legal, Compliance, Cybersecurity, Data &amp; Analytics, Infrastructure &amp; Cloud, and external technology partners to translate business priorities into scalable, secure, compliant, and sustainable technology solutions.</p>\n<p>The role combines strong technical expertise with application ownership and delivery leadership. The Senior Manager leads solution delivery from requirements and design through implementation and ongoing support, maintains sufficient hands-on expertise to independently assess, configure, and troubleshoot complex Veeva solutions, and ensures internal and external delivery teams provide reliable, high-quality services.</p>\n<p>The successful candidate will be comfortable moving between business conversations and technical decisions, understanding stakeholder priorities, shaping solutions, managing delivery and operational outcomes, and engaging directly with the technology when deeper expertise is required.</p>\n<p>&nbsp;</p>\n<p>&nbsp;</p>\n<h3>Position Responsibilities:</h3>\n</div>","descriptionBodyPlain":"The Senior Manager, Veeva Commercial & Data serves as the technology lead for enterprise applications and data supporting Scholar Rock’s Commercial and Medical organizations. Scholar Rock is establishing the application and data foundation required to support commercial launch, customer engagement, content management, medical communications, and future business growth, with Veeva serving as a core strategic platform.\nReporting to the Senior Director, Commercial & Data, the Senior Manager partners closely with Commercial, Medical Affairs, Commercial Operations, Regulatory, Legal, Compliance, Cybersecurity, Data & Analytics, Infrastructure & Cloud, and external technology partners to translate business priorities into scalable, secure, compliant, and sustainable technology solutions.\nThe role combines strong technical expertise with application ownership and delivery leadership. The Senior Manager leads solution delivery from requirements and design through implementation and ongoing support, maintains sufficient hands-on expertise to independently assess, configure, and troubleshoot complex Veeva solutions, and ensures internal and external delivery teams provide reliable, high-quality services.\nThe successful candidate will be comfortable moving between business conversations and technical decisions, understanding stakeholder priorities, shaping solutions, managing delivery and operational outcomes, and engaging directly with the technology when deeper expertise is required.\n \n \nPosition Responsibilities:\n","hostedUrl":"https://jobs.lever.co/scholarrock/3943729b-ad49-4a26-aa88-be59e2dac0e5","applyUrl":"https://jobs.lever.co/scholarrock/3943729b-ad49-4a26-aa88-be59e2dac0e5/apply"},{"additionalPlain":"Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. \n","additional":"<div><em>Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees</em>.&nbsp;</div>","categories":{"commitment":"Full-Time","department":"G&A","location":"Cambridge, MA","team":"Information Technology","allLocations":["Cambridge, MA"]},"createdAt":1786472038252,"descriptionPlain":"Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at ScholarRock.com and follow @ScholarRock on X and on LinkedIn.\n \nSummary of Position:\n\n\nThe Senior Manager, Veeva Regulatory & Data serves as the technology lead for enterprise applications and data supporting Scholar Rock’s Quality, Clinical, Regulatory, and Safety organizations. Scholar Rock has established a strong foundation of GxP applications and technology capabilities, with Veeva serving as a core strategic platform. This role will help mature, scale, and operationalize that foundation as the company advances through late-stage development, commercialization readiness, and global growth.\nReporting to the Senior Director, Commercial & Data, the Senior Manager partners closely with business stakeholders, Quality and Validation, Cybersecurity, Data & Analytics, Infrastructure & Cloud, and external technology partners to translate business priorities into scalable, secure, compliant, and sustainable technology solutions.\nThe role combines strong technical expertise with application ownership and delivery leadership. The Senior Manager leads solution delivery from requirements and design through implementation and ongoing support, maintains sufficient hands-on expertise to independently assess, configure, and troubleshoot complex Veeva solutions, and ensures internal and external delivery teams provide reliable, high-quality services.\nThe successful candidate will be comfortable moving between business conversations and technical decisions - understanding stakeholder priorities, shaping solutions, managing delivery and operational outcomes, and engaging directly with the technology when deeper expertise is required.\n \n \nPosition Responsibilities\n","description":"<div><em>Scholar Rock is a late-stage <span data-ogsc=\"red\">global&nbsp;</span>biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity.&nbsp;Scholar Rock&nbsp;works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at </em><a rel=\"noopener noreferrer\" href=\"http://www.scholarrock.com/\" class=\"postings-link\"><em>ScholarRock.com</em></a><em> and follow </em><a rel=\"noopener noreferrer\" href=\"http://www.twitter.com/scholarrock\" class=\"postings-link\"><em>@ScholarRock</em></a><em> on X and on&nbsp;</em><a rel=\"noopener noreferrer\" href=\"https://www.linkedin.com/company/scholar-rock\" class=\"postings-link\"><em>LinkedIn</em></a><em>.</em></div>\n<div>&nbsp;</div>\n<div><strong style=\"font-size: 18px;\">Summary of Position:</strong></div><div><br></div><div>\n<p>The <strong>Senior Manager, Veeva Regulatory &amp; Data</strong> serves as the technology lead for enterprise applications and data supporting Scholar Rock’s Quality, Clinical, Regulatory, and Safety organizations. Scholar Rock has established a strong foundation of GxP applications and technology capabilities, with Veeva serving as a core strategic platform. This role will help mature, scale, and operationalize that foundation as the company advances through late-stage development, commercialization readiness, and global growth.</p>\n<p>Reporting to the Senior Director, Commercial &amp; Data, the Senior Manager partners closely with business stakeholders, Quality and Validation, Cybersecurity, Data &amp; Analytics, Infrastructure &amp; Cloud, and external technology partners to translate business priorities into scalable, secure, compliant, and sustainable technology solutions.</p>\n<p>The role combines strong technical expertise with application ownership and delivery leadership. The Senior Manager leads solution delivery from requirements and design through implementation and ongoing support, maintains sufficient hands-on expertise to independently assess, configure, and troubleshoot complex Veeva solutions, and ensures internal and external delivery teams provide reliable, high-quality services.</p>\n<p>The successful candidate will be comfortable moving between business conversations and technical decisions - understanding stakeholder priorities, shaping solutions, managing delivery and operational outcomes, and engaging directly with the technology when deeper expertise is required.</p>\n<p>&nbsp;</p>\n<p>&nbsp;</p>\n<h3>Position Responsibilities</h3>\n</div>","id":"f6cc4cae-8d0f-4bad-8060-ce53be31b71d","lists":[{"text":"Business Partnership & Solution Delivery","content":"\n<li>Serve as a trusted technology partner to Quality, Clinical, Regulatory, and Safety stakeholders, developing a strong understanding of business priorities, processes, and evolving technology needs.</li>\n<li>Translate business and regulatory requirements into solution options, technical requirements, delivery plans, and measurable outcomes.</li>\n<li>Partner with the Senior Manager, Veeva Commercial and Data to execute the platform roadmap and align demand, priorities, dependencies, and delivery sequencing.</li>\n<li>Lead implementations, enhancements, integrations, releases, and continuous improvement initiatives across the GxP application portfolio.</li>\n<li>Communicate solution recommendations, delivery status, risks, dependencies, and tradeoffs clearly to business and technology stakeholders.</li>\n<li>Partner with business stakeholders to improve data quality, data stewardship, reporting enablement, and the effective use of application data supporting GxP business processes.</li>\n<li>Operate with a high degree of independence and judgment, making day-to-day application, technical, delivery, and operational decisions within established platform strategy and governance.</li>\n"},{"text":"Application & Technical Leadership","content":"\n<li>Provide technical leadership for Veeva and related GxP applications across solution design, configuration, integration, security, and lifecycle management.</li>\n<li>Design and configure complex Veeva Vault solutions when needed and maintain the technical depth required to troubleshoot issues, assess alternatives, and independently validate partner recommendations.</li>\n<li>Establish scalable configuration, integration, security, and release practices that improve consistency, maintainability, and supportability.</li>\n<li>Lead technical design for integrations between Veeva and adjacent applications, data platforms, identity services, middleware, APIs, and other regulated technologies.</li>\n<li>Partner with Cybersecurity, Data &amp; Analytics, Infrastructure &amp; Cloud, Quality, and Validation to ensure solutions align with enterprise standards and regulatory requirements.</li>\n"},{"text":"Application Lifecycle & Operational Excellence","content":"\n<li>Own the day-to-day health, performance, supportability, and service quality of assigned GxP applications.</li>\n<li>Ensure applications remain reliable, secure, compliant, scalable, and aligned with changing business requirements.</li>\n<li>Lead release planning, impact assessments, change execution, deployment readiness, and post-production support.</li>\n<li>Establish and monitor application health, service, delivery, quality, and adoption measures and use them to drive continuous improvement.</li>\n<li>Identify recurring issues, technical debt, lifecycle risks, and service gaps and drive appropriate remediation.</li>\n<li>Ensure effective incident, problem, change, enhancement, and escalation management across applications within scope.</li>\n"},{"text":"Vendor & Delivery Management","content":"\n<li>Lead managed service providers, systems integrators, consultants, and other external partners supporting the GxP application portfolio.</li>\n<li>Establish clear service, delivery, technical, and quality expectations and hold partners accountable for outcomes.</li>\n<li>Review and challenge vendor recommendations and technical solutions, ensuring decisions align with business requirements, architecture standards, and long-term application strategy.</li>\n<li>Manage delivery priorities, dependencies, escalations, risks, and performance across internal and external resources.</li>\n<li>Ensure effective documentation, knowledge transfer, operational readiness, and support transition for new and changed solutions.</li>\n<li>Build internal application knowledge and capability while using external partners strategically for capacity and specialized expertise.</li>\n"},{"text":"GxP, Validation & Compliance","content":"\n<li>Maintain the technical validated state of assigned applications and ensure changes remain appropriately controlled throughout the application lifecycle.</li>\n<li>Partner with Quality and Validation on validation strategy, impact assessment, testing, technical documentation, and remediation.</li>\n<li>Ensure solutions appropriately address applicable GxP requirements, electronic records and signatures, data integrity, access controls, audit trails, and regulated change requirements.</li>\n<li>Support regulatory inspections and audits and coordinate technical response and remediation for application-related observations.</li>\n<li>Promote practical, risk-based validation and compliance practices that support both regulatory expectations and sustainable technology delivery.</li>\n"},{"text":"Knowledge & Skills","content":"\n<li>Strong hands-on knowledge of Veeva Vault architecture, configuration, integrations, security, and application lifecycle management.</li>\n<li>Strong understanding of enterprise application delivery, operations, support, and service management.</li>\n<li>Demonstrated ability to translate business requirements into practical technology solutions and successfully lead those solutions through implementation and operation.</li>\n<li>Experience managing vendor-delivered technology services and providing technical oversight to systems integrators and managed service providers.</li>\n<li>Strong working knowledge of regulated GxP technology environments, computerized system validation, data integrity, and inspection-readiness expectations.</li>\n<li>Ability to independently assess complex business and technical issues, make sound decisions, resolve ambiguity, and engage specialized expertise when appropriate.</li>\n<li>Strong stakeholder management, communication, prioritization, problem-solving, and decision-making skills.</li>\n<li>Ability to balance business priorities, technical sustainability, regulatory requirements, operational risk, and delivery commitments.</li>\n"},{"text":"Candidate Qualifications ","content":"\n<li style=\"list-style-type: none;\">\n<ul type=\"disc\">\n<li>Bachelor's degree or equivalent combination of education and relevant experience.</li>\n<li>8+ years of progressive experience in enterprise applications, technology delivery, application management, or related disciplines, preferably within pharmaceutical, biotechnology, or life sciences.</li>\n<li>4+ years of hands-on experience implementing, configuring, supporting, or delivering Veeva Vault solutions across Quality, Clinical, Regulatory, Safety, or related regulated functions.</li>\n<li>Experience across Veeva Vault applications supporting Quality, Clinical, Regulatory, and Safety, such as QualityDocs, QMS, Training, Clinical Operations, RIM, and Safety.</li>\n<li>Experience leading implementations, enhancements, integrations, releases, and operational support for enterprise applications in validated GxP environments.</li>\n<li>Experience managing technology delivery involving managed service providers, systems integrators, consultants, or vendor-delivered solutions.</li>\n<li>Experience serving as a platform owner, technical lead, solution delivery lead, or comparable technology leadership role supporting regulated applications.</li>\n<li>Experience establishing trusted relationships with business stakeholders and translating complex business and regulatory needs into technology outcomes.</li>\n<li>Demonstrated ability to independently assess complex business and technical issues, make sound decisions, resolve ambiguity, and drive solutions through implementation and ongoing operation.</li>\n<li>Working knowledge of pharmaceutical regulatory requirements as applied to technology, including 21 CFR Part 11, computerized system validation, data integrity, and inspection readiness.</li>\n<li>Veeva Vault certification or advanced experience across multiple Veeva applications.</li>\n<li>Deep familiarity with the Veeva ecosystem (Vault, Network) and its data integration patterns.</li>\n<li>Experience leading application delivery teams, platform teams.</li>\n<li>Experience supporting data quality, data stewardship, reporting enablement, or data governance initiatives within regulated environments.</li>\n<li>Experience applying CSA principles and risk-based validation approaches.</li>\n<li>Experience integrating Veeva with ERP, data and analytics, middleware, identity, clinical, regulatory, or quality platforms; SAP experience is a plus.</li>\n<li>Prior experience in rare disease, specialty pharma, or biotechnology supporting regulated R&amp;D and Quality operations.</li>\n<li>Experience supporting late-stage clinical development, commercialization readiness, and the growth of global regulated operations within a biotechnology or pharmaceutical organization.</li>\n<li>ITIL, Product Management, Agile, Project Management, or related certifications preferred.</li>\n\n\n</ul></li>"}],"salaryRange":{"min":155000,"max":195000,"currency":"USD","interval":"per-year-salary"},"text":"Senior Manager, Veeva Regulatory & Data","country":"US","workplaceType":"onsite","opening":"<div><em>Scholar Rock is a late-stage <span data-ogsc=\"red\">global&nbsp;</span>biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity.&nbsp;Scholar Rock&nbsp;works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at </em><a class=\"postings-link\" href=\"http://www.scholarrock.com/\" target=\"_blank\" rel=\"noopener noreferrer\"><em>ScholarRock.com</em></a><em> and follow </em><a class=\"postings-link\" href=\"http://www.twitter.com/scholarrock\" target=\"_blank\" rel=\"noopener noreferrer\"><em>@ScholarRock</em></a><em> on X and on&nbsp;</em><a class=\"postings-link\" href=\"https://www.linkedin.com/company/scholar-rock\" target=\"_blank\" rel=\"noopener noreferrer\"><em>LinkedIn</em></a><em>.</em></div>\n<div>&nbsp;</div>\n<div><strong style=\"font-size: 18px;\">Summary of Position:</strong></div>","openingPlain":"Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at ScholarRock.com and follow @ScholarRock on X and on LinkedIn.\n \nSummary of Position:\n","descriptionBody":"<div>\n<p>The <strong>Senior Manager, Veeva Regulatory &amp; Data</strong> serves as the technology lead for enterprise applications and data supporting Scholar Rock&rsquo;s Quality, Clinical, Regulatory, and Safety organizations. Scholar Rock has established a strong foundation of GxP applications and technology capabilities, with Veeva serving as a core strategic platform. This role will help mature, scale, and operationalize that foundation as the company advances through late-stage development, commercialization readiness, and global growth.</p>\n<p>Reporting to the Senior Director, Commercial &amp; Data, the Senior Manager partners closely with business stakeholders, Quality and Validation, Cybersecurity, Data &amp; Analytics, Infrastructure &amp; Cloud, and external technology partners to translate business priorities into scalable, secure, compliant, and sustainable technology solutions.</p>\n<p>The role combines strong technical expertise with application ownership and delivery leadership. The Senior Manager leads solution delivery from requirements and design through implementation and ongoing support, maintains sufficient hands-on expertise to independently assess, configure, and troubleshoot complex Veeva solutions, and ensures internal and external delivery teams provide reliable, high-quality services.</p>\n<p>The successful candidate will be comfortable moving between business conversations and technical decisions - understanding stakeholder priorities, shaping solutions, managing delivery and operational outcomes, and engaging directly with the technology when deeper expertise is required.</p>\n<p>&nbsp;</p>\n<p>&nbsp;</p>\n<h3>Position Responsibilities</h3>\n</div>","descriptionBodyPlain":"The Senior Manager, Veeva Regulatory & Data serves as the technology lead for enterprise applications and data supporting Scholar Rock’s Quality, Clinical, Regulatory, and Safety organizations. Scholar Rock has established a strong foundation of GxP applications and technology capabilities, with Veeva serving as a core strategic platform. This role will help mature, scale, and operationalize that foundation as the company advances through late-stage development, commercialization readiness, and global growth.\nReporting to the Senior Director, Commercial & Data, the Senior Manager partners closely with business stakeholders, Quality and Validation, Cybersecurity, Data & Analytics, Infrastructure & Cloud, and external technology partners to translate business priorities into scalable, secure, compliant, and sustainable technology solutions.\nThe role combines strong technical expertise with application ownership and delivery leadership. The Senior Manager leads solution delivery from requirements and design through implementation and ongoing support, maintains sufficient hands-on expertise to independently assess, configure, and troubleshoot complex Veeva solutions, and ensures internal and external delivery teams provide reliable, high-quality services.\nThe successful candidate will be comfortable moving between business conversations and technical decisions - understanding stakeholder priorities, shaping solutions, managing delivery and operational outcomes, and engaging directly with the technology when deeper expertise is required.\n \n \nPosition Responsibilities\n","hostedUrl":"https://jobs.lever.co/scholarrock/f6cc4cae-8d0f-4bad-8060-ce53be31b71d","applyUrl":"https://jobs.lever.co/scholarrock/f6cc4cae-8d0f-4bad-8060-ce53be31b71d/apply"},{"additionalPlain":"Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. \n","additional":"<div><em>Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees</em>.&nbsp;</div>","categories":{"commitment":"Full-Time","department":"Commercial","location":"Remote","team":"Global Medical Affairs","allLocations":["Remote"]},"createdAt":1775486063615,"descriptionPlain":"Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at ScholarRock.com and follow @ScholarRock on X and on LinkedIn.\n \nSummary of Position:\n\n\nThe Sr MSL role will represent the real time voice of KOL/HCP input related product development opportunities and scientific exchange on pipeline and commercial products; conduct clinical presentations to payer organizations.  The ideal candidate will be a strong leader with a proven ability to leverage their high scientific acumen to engaged and educate on scientifically complex concepts and products. The preferred candidate will also have a proven strategic and innovative style combined with a flexible, hands-on nature that works with a high sense of urgency.\n","description":"<div><em>Scholar Rock is a late-stage <span data-ogsc=\"red\">global&nbsp;</span>biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity.&nbsp;Scholar Rock&nbsp;works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at </em><a rel=\"noopener noreferrer\" href=\"http://www.scholarrock.com/\" class=\"postings-link\"><em>ScholarRock.com</em></a><em> and follow </em><a rel=\"noopener noreferrer\" href=\"http://www.twitter.com/scholarrock\" class=\"postings-link\"><em>@ScholarRock</em></a><em> on X and on&nbsp;</em><a rel=\"noopener noreferrer\" href=\"https://www.linkedin.com/company/scholar-rock\" class=\"postings-link\"><em>LinkedIn</em></a><em>.</em></div>\n<div>&nbsp;</div>\n<div><strong style=\"font-size: 18px;\">Summary of Position:</strong></div><div><br></div><div>The Sr MSL role will represent the real time voice of KOL/HCP input related product development opportunities and scientific exchange on pipeline and commercial products; conduct clinical presentations to payer organizations. &nbsp;The ideal candidate will be a strong leader with a proven ability to leverage their high scientific acumen to engaged and educate on scientifically complex concepts and products. The preferred candidate will also have a proven strategic and innovative style combined with a flexible, hands-on nature that works with a high sense of urgency.</div>","id":"cef7149a-d0d1-465d-8015-0db2f7f7ee04","lists":[{"text":"Position Responsibilities","content":"\n<li>Become a SMA and apitegromab medical/clinical/scientific expert</li>\n<li>Build and foster relationships with local, regional, and national KOLs and possibly Payers</li>\n<li>Effectively deliver medical/clinical/scientific presentations to a diverse external audience</li>\n<li>Support clinical development activities, investigator recruitment and education</li>\n<li>Development and execution of their Territory Management Plan (TMP) that is aligned with the overall Medical Goals and Plan</li>\n<li>Contribute to developing metrics, qualitative and quantitative MSL reports, SOPs/Business Practices for the MSL function</li>\n<li>Responding to unsolicited medical information requests submitted by SRRK field teams (eg. Sales and Market Access)&nbsp;</li>\n<li>Compliantly partner with Sales and Market Access on high-level regional engagement</li>\n<li>Provide internal teams with insights from interactions and discussions with HCPs</li>\n<li>Co-create and deliver the MSL training</li>\n<li>Provide content development support for MSL materials, alongside the Director of Medical Communications</li>\n<li>Contribute to the development of the Global and US Medical Plans for apitegromab in SMA</li>\n<li>May be asked to participate in Advisory Board meeting, Advisory Group meetings, speaker trainings, etc.</li>\n<li>Coordinate local and regional investigator-initiated research (IIR)</li>\n<li>Compliantly manage IIR milestones and objectives</li>\n<li>Report on scientific sessions and conduct scientific exchange to unsolicited questions at SRRK medical booths at congresses</li>\n<li>May respond to and document unsolicited requests for scientific information</li>\n<li>Conduct all activities and responsibilities in accordance with all relevant legal, regulatory and corporate regulations and guidelines, including the Scholar Rock Business Conduct &amp; Ethics, policies and procedures</li>\n"},{"text":"Candidate Requirements","content":"\n<li>MD, PharmD, or PhD preferred. &nbsp;Advanced professional degree (NP, PT etc) may be considered for candidates with significant clinical neuromuscular disease experience</li>\n<li>Neurology and/or rare disease experience with prior launch experience preferred</li>\n<li>Demonstrated knowledge of regulatory, commercial and clinical issues affecting the pharmaceutical industry is critical</li>\n<li>Excellent verbal and written communication, presentation, and interpersonal skills are essential</li>\n<li>Demonstrated strategic planning, organizational and project management abilities are required</li>\n<li>Ability to collaborate in a team environment and partner effectively across geographic areas and cross-functional groups is essential</li>\n<li>Experience in at least one “start-up” biopharma company is desirable.</li>\n<li>Must be passionate about making a difference with the highest integrity; committed to ethics and scientific standards</li>\n<li>Demonstrated ability to work independently yet engage in collaborative decision making to complete tasks in a timely fashion, and function in a rapidly paced environment</li>\n<li>Experience with customer relationship management programs a plus</li>\n<li>This will be a remote position that will require extensive overnight travel (&gt;50%).&nbsp;</li>\n"}],"salaryRange":{"min":220000,"max":250000,"currency":"USD","interval":"per-year-salary"},"text":"Senior Medical Science Liaison- Great Lakes","country":"US","workplaceType":"remote","opening":"<div><em>Scholar Rock is a late-stage <span data-ogsc=\"red\">global&nbsp;</span>biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity.&nbsp;Scholar Rock&nbsp;works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at </em><a class=\"postings-link\" href=\"http://www.scholarrock.com/\" target=\"_blank\" rel=\"noopener noreferrer\"><em>ScholarRock.com</em></a><em> and follow </em><a class=\"postings-link\" href=\"http://www.twitter.com/scholarrock\" target=\"_blank\" rel=\"noopener noreferrer\"><em>@ScholarRock</em></a><em> on X and on&nbsp;</em><a class=\"postings-link\" href=\"https://www.linkedin.com/company/scholar-rock\" target=\"_blank\" rel=\"noopener noreferrer\"><em>LinkedIn</em></a><em>.</em></div>\n<div>&nbsp;</div>\n<div><strong style=\"font-size: 18px;\">Summary of Position:</strong></div>","openingPlain":"Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at ScholarRock.com and follow @ScholarRock on X and on LinkedIn.\n \nSummary of Position:\n","descriptionBody":"<div>The Sr MSL role will represent the real time voice of KOL/HCP input related product development opportunities and scientific exchange on pipeline and commercial products; conduct clinical presentations to payer organizations. &nbsp;The ideal candidate will be a strong leader with a proven ability to leverage their high scientific acumen to engaged and educate on scientifically complex concepts and products. The preferred candidate will also have a proven strategic and innovative style combined with a flexible, hands-on nature that works with a high sense of urgency.</div>","descriptionBodyPlain":"The Sr MSL role will represent the real time voice of KOL/HCP input related product development opportunities and scientific exchange on pipeline and commercial products; conduct clinical presentations to payer organizations.  The ideal candidate will be a strong leader with a proven ability to leverage their high scientific acumen to engaged and educate on scientifically complex concepts and products. The preferred candidate will also have a proven strategic and innovative style combined with a flexible, hands-on nature that works with a high sense of urgency.\n","hostedUrl":"https://jobs.lever.co/scholarrock/cef7149a-d0d1-465d-8015-0db2f7f7ee04","applyUrl":"https://jobs.lever.co/scholarrock/cef7149a-d0d1-465d-8015-0db2f7f7ee04/apply"},{"additionalPlain":"Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. \n","additional":"<div><em>Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees</em>.&nbsp;</div>","categories":{"commitment":"Full-Time","department":"Development","location":"Zug","team":"Global Quality","allLocations":["Zug"]},"createdAt":1782736377113,"descriptionPlain":"Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at ScholarRock.com and follow @ScholarRock on X and on LinkedIn.\n \nSummary of Position:\n","description":"<div><em>Scholar Rock is a late-stage <span data-ogsc=\"red\">global&nbsp;</span>biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity.&nbsp;Scholar Rock&nbsp;works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at </em><a rel=\"noopener noreferrer\" href=\"http://www.scholarrock.com/\" class=\"postings-link\"><em>ScholarRock.com</em></a><em> and follow </em><a rel=\"noopener noreferrer\" href=\"http://www.twitter.com/scholarrock\" class=\"postings-link\"><em>@ScholarRock</em></a><em> on X and on&nbsp;</em><a rel=\"noopener noreferrer\" href=\"https://www.linkedin.com/company/scholar-rock\" class=\"postings-link\"><em>LinkedIn</em></a><em>.</em></div>\n<div>&nbsp;</div>\n<div><strong style=\"font-size: 18px;\">Summary of Position:</strong></div><div><br></div><div>\n<p>Scholar Rock is seeking an experienced and motivated Senior Director, Commercial Quality / Market Quality (Switzerland) to build and lead a phase-appropriate, scalable, and inspection-ready Commercial Quality function as Scholar Rock advances to and expands in commercial supply. Reporting to the Head of Global Quality, this role is the Quality leader accountable for establishing clear separation between manufacturing control and commercial control through creation of a dedicated Market Release Authorization vertical, ensuring compliant disposition for each market and reliable supply to patients.</p>\n<p>Based in Switzerland, the Senior Director, Commercial Quality is accountable for EU/EEA-aligned commercial quality governance, including oversight of QP certification and market release readiness (where applicable), and for establishing the authority to place and lift commercial holds (including for safety, distribution, shortage mitigation, and recall/field action reasons). This leader will create robust post-market controls that meet FDA, European/Swiss expectations (and ROW in market requirements) to ensure compliant product release, complaint handling, investigations/CAPA, and effective management of quality risks in the marketplace.&nbsp;</p>\n</div>","id":"cb95ccc4-79f3-429e-ae88-cbf7fa51bb3d","lists":[{"text":"Position Responsibilities ","content":"\n<li>Provide senior leadership for Commercial Quality, ensuring patient-focused, compliant, and robust oversight of marketed product(s) and launch readiness for new indications/markets.</li>\n<li>Establish and own the Market Release Authorization vertical, distinguishing manufacturing batch disposition from commercial/market disposition and ensuring release decisions meet applicable market requirements (U.S., EU, and other regions as expanded).</li>\n<li>Serve as the end-to-end Quality leader for commercial operations, partnering with Supply Chain, Distribution/Logistics, Labeling, Regulatory, Pharmacovigilance, Medical Affairs, and Manufacturing/CMOs to enable reliable supply and compliant market execution.</li>\n<li>Hold decision rights to place and lift commercial holds, including for safety signals, distribution excursions, labeling issues, complaint trends, shortage mitigation, or recall-related actions; ensure clear governance, escalation pathways, and documentation.</li>\n<li>Own and continuously improve the post-market quality system to meet health authority expectations as per applicable guidance, and to support global regulatory commitments.</li>\n<li>Lead commercial product release/disposition governance, including product status control, release documentation, country-specific requirements, and oversight of release by Qualified Person (QP) (as applicable), governance of batch certification packages and escalation pathways for quality decisions.</li>\n<li>Provide Quality oversight for distribution and logistics, including EU GDP expectations, temperature-controlled/cold chain processes, lane qualification, distribution excursions/investigations, returns/destruction, and oversight of 3PLs and other service providers across Switzerland, EU/EEA, and other regions through quality agreements and metrics.</li>\n<li>Lead commercial Quality inspection readiness and external interactions, including health authority inspections, ensuring sustained compliance across the commercial supply chain.</li>\n<li>Lead and execute recall and field action readiness and response (including mock recalls), partnering with PV/Medical/Regulatory and Supply Chain to ensure timely decisions, effective communications, and compliant execution (including EU/UK-style Field Safety Corrective Actions where applicable).</li>\n<li>Oversee quality impact assessment and decision-making for changes that may affect marketed product (process, analytical, specifications, site/supplier, packaging/labeling, distribution lanes), ensuring alignment with filings/commitments and market release requirements.</li>\n<li>Provide governance for commercial packaging and labeling quality (artwork/label content controls, printed component release, reconciliation, tamper evidence), and partner with Regulatory Labeling to ensure compliant implementation across markets.</li>\n<li>Partner with Supply Chain/IT and external providers to ensure compliance with applicable serialization/traceability requirements and robust product security controls, as needed by market.</li>\n"},{"text":"Candidate Requirements","content":"\n<li>BS/BA degree in a scientific or engineering discipline required; advanced degree preferred</li>\n<li>15+ years of progressive Quality experience in biotech/pharma (biologics preferred), including significant leadership of commercial quality and oversight of external manufacturing, packaging/labeling, testing, and distribution networks; people leadership strongly preferred</li>\n<li>Demonstrated expertise with marketed product quality systems, including commercial batch release/market disposition, product status control, complaint handling, and quality risk management</li>\n<li>Strong working knowledge of European and Swissmedic regulations and guidance applicable to commercial supply; experience representing Quality in health authority inspections (e.g., EMA member state authorities, MHRA, Swissmedic, FDA)</li>\n<li>Hands-on experience operating within an EU/EEA commercial release model, including governance of QP certification activities and batch certification packages; prior direct QP qualification is a plus</li>\n<li>Experience establishing and governing post-market product monitoring, including complaint trending and signal detection interfaces with Pharmacovigilance/Medical, management review/KPIs, and continuous improvement</li>\n<li>Proven experience leading recalls/field actions, including decision-making, health authority notifications support, cross-functional execution, and effectiveness checks; experience conducting mock recalls preferred</li>\n<li>Demonstrated ability to lead through influence in a matrixed organization and drive effective governance across external partners (e.g., quality agreements, release expectations, GDP oversight, metrics/KPIs, escalation pathways, and performance improvement)</li>\n<li>Strong executive presence and communication skills, sound risk-based judgment, and the ability to balance strategic leadership with timely, compliant quality decision-making&nbsp;</li>\n<li>Highly proactive, decisive, and capable of independently driving complex cross-functional initiatives in a fast-paced environment; experience scaling commercial quality capabilities for European launch and expansion (including GDP networks and QP release models) and broader ex-U.S./ROW expansion strongly preferred</li>\n"}],"text":"Sr. Director, Commercial Quality / Market Quality","country":"CH","workplaceType":"onsite","opening":"<div><em>Scholar Rock is a late-stage <span data-ogsc=\"red\">global&nbsp;</span>biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity.&nbsp;Scholar Rock&nbsp;works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at </em><a class=\"postings-link\" href=\"http://www.scholarrock.com/\" target=\"_blank\" rel=\"noopener noreferrer\"><em>ScholarRock.com</em></a><em> and follow </em><a class=\"postings-link\" href=\"http://www.twitter.com/scholarrock\" target=\"_blank\" rel=\"noopener noreferrer\"><em>@ScholarRock</em></a><em> on X and on&nbsp;</em><a class=\"postings-link\" href=\"https://www.linkedin.com/company/scholar-rock\" target=\"_blank\" rel=\"noopener noreferrer\"><em>LinkedIn</em></a><em>.</em></div>\n<div>&nbsp;</div>\n<div><strong style=\"font-size: 18px;\">Summary of Position:</strong></div>","openingPlain":"Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at ScholarRock.com and follow @ScholarRock on X and on LinkedIn.\n \nSummary of Position:\n","descriptionBody":"<div>\n<p>Scholar Rock is seeking an experienced and motivated Senior Director, Commercial Quality / Market Quality (Switzerland) to build and lead a phase-appropriate, scalable, and inspection-ready Commercial Quality function as Scholar Rock advances to and expands in commercial supply. Reporting to the Head of Global Quality, this role is the Quality leader accountable for establishing clear separation between manufacturing control and commercial control through creation of a dedicated Market Release Authorization vertical, ensuring compliant disposition for each market and reliable supply to patients.</p>\n<p>Based in Switzerland, the Senior Director, Commercial Quality is accountable for EU/EEA-aligned commercial quality governance, including oversight of QP certification and market release readiness (where applicable), and for establishing the authority to place and lift commercial holds (including for safety, distribution, shortage mitigation, and recall/field action reasons). This leader will create robust post-market controls that meet FDA, European/Swiss expectations (and ROW in market requirements) to ensure compliant product release, complaint handling, investigations/CAPA, and effective management of quality risks in the marketplace.&nbsp;</p>\n</div>","descriptionBodyPlain":"","hostedUrl":"https://jobs.lever.co/scholarrock/cb95ccc4-79f3-429e-ae88-cbf7fa51bb3d","applyUrl":"https://jobs.lever.co/scholarrock/cb95ccc4-79f3-429e-ae88-cbf7fa51bb3d/apply"},{"additionalPlain":"Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. \n","additional":"<div><em>Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees</em>.&nbsp;</div>","categories":{"commitment":"Full-Time","department":"G&A","location":"Cambridge, MA","team":"Human Resources","allLocations":["Cambridge, MA"]},"createdAt":1780947066722,"descriptionPlain":"Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at ScholarRock.com and follow @ScholarRock on X and on LinkedIn.\n \nSummary of Position:\n","description":"<div><em>Scholar Rock is a late-stage <span data-ogsc=\"red\">global&nbsp;</span>biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity.&nbsp;Scholar Rock&nbsp;works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at </em><a rel=\"noopener noreferrer\" href=\"http://www.scholarrock.com/\" class=\"postings-link\"><em>ScholarRock.com</em></a><em> and follow </em><a rel=\"noopener noreferrer\" href=\"http://www.twitter.com/scholarrock\" class=\"postings-link\"><em>@ScholarRock</em></a><em> on X and on&nbsp;</em><a rel=\"noopener noreferrer\" href=\"https://www.linkedin.com/company/scholar-rock\" class=\"postings-link\"><em>LinkedIn</em></a><em>.</em></div>\n<div>&nbsp;</div>\n<div><strong style=\"font-size: 18px;\">Summary of Position:</strong></div><div><br></div><div><span data-contrast=\"auto\">The Human Resource Business Partner (HRBP) provides HR leadership and support to our Research &amp; Development and Tech Ops &amp; Quality organizations. The HRBP is a trusted advisor to leaders, providing expert HR advice and advanced solutions that enable the achievement of business strategies by leveraging effective people processes. This role drives talent, culture, change management and operational excellence for the US &amp; Global organizations, overseeing the delivery of HR programs and services such as leadership, talent acquisition &amp; talent management including employee development, coaching, compensation processes, performance management, organization and change management.&nbsp;&nbsp;This role will also lead Employee Relations processes and procedures to enable effective management, conflict resolution, and problem solving across these organizations. </span><span data-ccp-props=\"{}\">&nbsp;</span></div>","id":"6d8e5c9e-7895-4846-b6a4-09500fcaae59","lists":[{"text":"Position Responsibilities: ","content":"<div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"39\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"1\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Provides&nbsp;strategic HR leadership and expert guidance to&nbsp;our&nbsp;R&amp;D and TOQ&nbsp;organization&nbsp;for all&nbsp;people&nbsp;processes,&nbsp;delivering&nbsp;HR programs&nbsp;and services to achieve key business&nbsp;objectives.&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"39\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"2\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Proactively defines,&nbsp;builds&nbsp;and implements value-added HR strategies and solutions&nbsp;based on the needs of the organization; advising&nbsp;functional leaders in solving complex issues related to organization design, development, and change leadership.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"39\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"3\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Partner with Talent teams&nbsp;to&nbsp;establish&nbsp;strategies and tactics to deliver the people and talent strategy for the&nbsp;R&amp;D and TOQ&nbsp;organizations&nbsp;including&nbsp;the&nbsp;attraction, development, and retention of&nbsp;high-quality talent&nbsp;aligned with growth&nbsp;objectives,&nbsp;long-term capability needs,&nbsp;and corporate strategy.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"39\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"4\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Builds strong partnerships with the HR specialist functions&nbsp;to&nbsp;provide HR solutions to key business needs and to roll out programs that enhance overall employee engagement&nbsp;and organization change initiatives.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"39\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"5\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Implement and manage key HR processes, such as the year-end performance management process (performance assessment, calibration, and compensation planning).</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"39\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"6\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Manage&nbsp;employee relation issues to&nbsp;understand&nbsp;employee concerns,&nbsp;identify&nbsp;and implement&nbsp;appropriate employee&nbsp;action and accountability practices.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"39\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"7\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Provides&nbsp;guidance and coaching to managers of all levels to address employee behavior and&nbsp;performance&nbsp;and&nbsp;assisting&nbsp;with the development and delivery of&nbsp;appropriate performance&nbsp;feedback or action plans including corrective/disciplinary actions.</span></p>\n</li>\n\n</ul></div>\n</div>"},{"text":"Candidate Requirements:","content":"<div>\n<div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"37\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"1\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">10&nbsp;years of experience&nbsp;or equivalent combination of education with experience in HR business partnering&nbsp;or related discipline&nbsp;with&nbsp;deep understanding of biotech/pharma industry.&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"37\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"2\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Experience developing and implementing HR&nbsp;plans and&nbsp;strategies&nbsp;supporting&nbsp;R&amp;D functions&nbsp;is&nbsp;a must.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"37\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"3\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Highly experienced in talent management, succession planning,&nbsp;leadership and employee&nbsp;development, employee relations,&nbsp;and&nbsp;employee engagement.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"37\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"4\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Strong experience managing and/or leading culture and&nbsp;change&nbsp;management or organizational effectiveness initiatives.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n</div>\n<div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"37\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"5\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Demonstrated&nbsp;employee relations&nbsp;expertise, excellent judgment, and highly developed analytical, interpersonal, problem-solving and communication skills.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"37\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"6\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Ability to distill complex information into key messages, clearly and simply&nbsp;communicating&nbsp;in a compelling way to all levels&nbsp;of an organization</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"38\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"1\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Experience in leading large-scale projects, comfortable driving&nbsp;change&nbsp;and embracing innovation in the face of ambiguity and complexity.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"38\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"2\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">A leader who is values-driven and able and willing to work at all levels.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n</div>\n</div>"}],"salaryRange":{"min":265000,"max":300000,"currency":"USD","interval":"per-year-salary"},"text":"Sr. Director, HR Business Partner (R & D and Tech Ops & Quality)","country":"US","workplaceType":"onsite","opening":"<div><em>Scholar Rock is a late-stage <span data-ogsc=\"red\">global&nbsp;</span>biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity.&nbsp;Scholar Rock&nbsp;works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at </em><a class=\"postings-link\" href=\"http://www.scholarrock.com/\" target=\"_blank\" rel=\"noopener noreferrer\"><em>ScholarRock.com</em></a><em> and follow </em><a class=\"postings-link\" href=\"http://www.twitter.com/scholarrock\" target=\"_blank\" rel=\"noopener noreferrer\"><em>@ScholarRock</em></a><em> on X and on&nbsp;</em><a class=\"postings-link\" href=\"https://www.linkedin.com/company/scholar-rock\" target=\"_blank\" rel=\"noopener noreferrer\"><em>LinkedIn</em></a><em>.</em></div>\n<div>&nbsp;</div>\n<div><strong style=\"font-size: 18px;\">Summary of Position:</strong></div>","openingPlain":"Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at ScholarRock.com and follow @ScholarRock on X and on LinkedIn.\n \nSummary of Position:\n","descriptionBody":"<div><span xml:lang=\"EN-US\" data-contrast=\"auto\">The Human Resource Business Partner (HRBP) provides HR leadership and support to our Research &amp; Development and Tech Ops &amp; Quality organizations. The HRBP is a trusted advisor to leaders, providing expert HR advice and advanced solutions that enable the achievement of business strategies by leveraging effective people processes. This role drives talent, culture, change management and operational excellence for the US &amp; Global organizations, overseeing the delivery of HR programs and services such as leadership, talent acquisition &amp; talent management including employee development, coaching, compensation processes, performance management, organization and change management.&nbsp;&nbsp;This role will also lead Employee Relations processes and procedures to enable effective management, conflict resolution, and problem solving across these organizations. </span><span data-ccp-props=\"{}\">&nbsp;</span></div>","descriptionBodyPlain":"","hostedUrl":"https://jobs.lever.co/scholarrock/6d8e5c9e-7895-4846-b6a4-09500fcaae59","applyUrl":"https://jobs.lever.co/scholarrock/6d8e5c9e-7895-4846-b6a4-09500fcaae59/apply"},{"additionalPlain":"Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. \n","additional":"<div><em>Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees</em>.&nbsp;</div>","categories":{"commitment":"Full-Time","department":"Development","location":"Cambridge, MA","team":"Regulatory Affairs","allLocations":["Cambridge, MA"]},"createdAt":1773670995433,"descriptionPlain":"Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at ScholarRock.com and follow @ScholarRock on X and on LinkedIn.\n \nSummary of Position:\n\n\nThe Director or Senior Director, Regulatory Strategy, reporting to the SVP, Global Head of Regulatory Affairs, is responsible for the development and implementation of the Global Strategy for assigned clinical and/or pipeline programs globally depending on the program. As a subject matter expert, this individual will represent regulatory affairs at the appropriate program team, highlighting risks and opportunities to inform program strategy and plan. The successful candidate will lead interactions with the regulatory authorities, directing the preparation and submission of regulatory submissions and correspondence.\n","description":"<div><em>Scholar Rock is a late-stage <span data-ogsc=\"red\">global&nbsp;</span>biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity.&nbsp;Scholar Rock&nbsp;works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at </em><a rel=\"noopener noreferrer\" href=\"http://www.scholarrock.com/\" class=\"postings-link\"><em>ScholarRock.com</em></a><em> and follow </em><a rel=\"noopener noreferrer\" href=\"http://www.twitter.com/scholarrock\" class=\"postings-link\"><em>@ScholarRock</em></a><em> on X and on&nbsp;</em><a rel=\"noopener noreferrer\" href=\"https://www.linkedin.com/company/scholar-rock\" class=\"postings-link\"><em>LinkedIn</em></a><em>.</em></div>\n<div>&nbsp;</div>\n<div><strong style=\"font-size: 18px;\">Summary of Position:</strong></div><div><br></div><div>The Director or Senior Director, Regulatory Strategy, reporting to the SVP, Global Head of Regulatory Affairs, is responsible for the development and implementation of the Global Strategy for assigned clinical and/or pipeline programs globally depending on the program. As a subject matter expert, this individual will represent regulatory affairs at the appropriate program team, highlighting risks and opportunities to inform program strategy and plan. The successful candidate will lead interactions with the regulatory authorities, directing the preparation and submission of regulatory submissions and correspondence.</div>","id":"d8a969dc-949a-4899-a7bf-49479ac68244","lists":[{"text":"Position Responsibilities","content":"\n<li>Serve as a thought leader on regulatory affairs, defining global regulatory strategy and plan to maximize regulatory success.</li>\n<li>Serve as the global regulatory lead, providing strategic and operational input on assigned clinical and/or pipeline programs, such as the subcutaneous (IV to SC) and OPAL (&lt;2 years old) program teams to achieve program objectives while ensuring compliance with applicable regulatory requirements in the region.</li>\n<li>Be responsible for leading the global supplemental/type 2 variation filing lead for OPAL (&lt;2 years old)</li>\n<li>Develop regulatory roadmap to inform and guide agency engagement strategy; partner with key stakeholders to develop and implement a comprehensive regulatory engagement plan</li>\n<li>Lead and managing regulatory interactions on assigned programs, building trusted relationships with regulatory authorities</li>\n<li>Lead cross-functional effort to ensure timely submission of key regulatory documents (e.g., Module 1, briefing documents)</li>\n<li>Ensure program team members and cross-functional stakeholders are informed of internal and external events that may impact regulatory success</li>\n<li>Identify regulatory risks and opportunities and work with key stakeholders to develop solutions</li>\n<li>Partner with global market access and medical affairs colleagues to support interactions with joint regulatory/health agency/HTA bodies on product specific value evidence topics, as applicable</li>\n<li>Partner with Global and local Marketing/ Commercial as needed to align Regulatory Plan and Marketing/Commercial plan</li>\n<li>Ensure strong representation of regulatory voice at key governance bodies and teams (e.g., DRC, program teams, clinical development teams, study teams)</li>\n<li>Maintain currency of regulatory requirements and approvals to inform regulatory strategies and drive proactive plans to ensure compliance</li>\n<li>Monitor and analyze global and country specific regulatory landscape to assess potential impact on the program; collaborate with teams to ensure compliance</li>\n<li>Provide support to local regulatory experts</li>\n<li>Provide regulatory support for cross-functional activities (e.g., SOPs, business development, clinical labeling, disclosure) as needed</li>\n"},{"text":"Candidate Requirements","content":"\n<li>Education in life sciences required</li>\n<li>Greater Boston-based with ability to be regularly present in the Cambridge, MA office</li>\n<li>7+ years of experience Regulatory Affairs in biopharmaceutical industry with deep understanding of EU regulatory requirements</li>\n<li>Demonstrated experience of leading successful engagement with EMA</li>\n<li>Expertise and experience with biologics (particularly monoclonal antibody therapeutics) and rare diseases strongly preferred but not required</li>\n<li>Demonstrated reputation as a well-respected, dynamic team leader with strong leadership and people management skills</li>\n<li>Strong written, verbal communication skills, and interpersonal skills</li>\n<li>Capable of managing shifting priorities in a rapidly changing and environment</li>\n<li>Ability to travel domestically and internationally (~10%)</li>\n"}],"salaryRange":{"min":200000,"max":300000,"currency":"USD","interval":"per-year-salary"},"text":"Sr. Director, Regulatory Strategy","country":"US","workplaceType":"hybrid","opening":"<div><em>Scholar Rock is a late-stage <span data-ogsc=\"red\">global&nbsp;</span>biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity.&nbsp;Scholar Rock&nbsp;works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at </em><a class=\"postings-link\" href=\"http://www.scholarrock.com/\" target=\"_blank\" rel=\"noopener noreferrer\"><em>ScholarRock.com</em></a><em> and follow </em><a class=\"postings-link\" href=\"http://www.twitter.com/scholarrock\" target=\"_blank\" rel=\"noopener noreferrer\"><em>@ScholarRock</em></a><em> on X and on&nbsp;</em><a class=\"postings-link\" href=\"https://www.linkedin.com/company/scholar-rock\" target=\"_blank\" rel=\"noopener noreferrer\"><em>LinkedIn</em></a><em>.</em></div>\n<div>&nbsp;</div>\n<div><strong style=\"font-size: 18px;\">Summary of Position:</strong></div>","openingPlain":"Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at ScholarRock.com and follow @ScholarRock on X and on LinkedIn.\n \nSummary of Position:\n","descriptionBody":"<div>The Director or Senior Director, Regulatory Strategy, reporting to the SVP, Global Head of Regulatory Affairs, is responsible for the development and implementation of the Global Strategy for assigned clinical and/or pipeline programs globally depending on the program. As a subject matter expert, this individual will represent regulatory affairs at the appropriate program team, highlighting risks and opportunities to inform program strategy and plan. The successful candidate will lead interactions with the regulatory authorities, directing the preparation and submission of regulatory submissions and correspondence.</div>","descriptionBodyPlain":"The Director or Senior Director, Regulatory Strategy, reporting to the SVP, Global Head of Regulatory Affairs, is responsible for the development and implementation of the Global Strategy for assigned clinical and/or pipeline programs globally depending on the program. As a subject matter expert, this individual will represent regulatory affairs at the appropriate program team, highlighting risks and opportunities to inform program strategy and plan. The successful candidate will lead interactions with the regulatory authorities, directing the preparation and submission of regulatory submissions and correspondence.\n","hostedUrl":"https://jobs.lever.co/scholarrock/d8a969dc-949a-4899-a7bf-49479ac68244","applyUrl":"https://jobs.lever.co/scholarrock/d8a969dc-949a-4899-a7bf-49479ac68244/apply"},{"additionalPlain":"Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. \n","additional":"<div><em>Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees</em>.&nbsp;</div>","categories":{"commitment":"Full-Time","department":"Development","location":"Cambridge, MA","team":"PV","allLocations":["Cambridge, MA"]},"createdAt":1752692684416,"descriptionPlain":"Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at ScholarRock.com and follow @ScholarRock on X and on LinkedIn.\n \nSummary of Position:\n\n\nThe Sr. Medical Director, Drug Safety & Pharmacovigilance is a key position within the company and safety department, with significant impact on the development and life cycle of drug development projects. Responsible for providing safety strategy, expertise, and guidance, pre- and post-approval for assigned products, the Sr. Medical Director will drive the proactive implementation of risk management initiatives in accordance with global regulatory requirements. Core responsibilities will encompass continuous and efficient evaluation of safety data, perform signal detection, evaluation and assessment and management of the safety profile of the compound. In addition, the position will work closely with cross functional teams and Departments for achieving project goals, within timelines & with high quality.\n","description":"<div><em>Scholar Rock is a late-stage <span data-ogsc=\"red\">global&nbsp;</span>biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity.&nbsp;Scholar Rock&nbsp;works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at </em><a rel=\"noopener noreferrer\" href=\"http://www.scholarrock.com/\" class=\"postings-link\"><em>ScholarRock.com</em></a><em> and follow </em><a rel=\"noopener noreferrer\" href=\"http://www.twitter.com/scholarrock\" class=\"postings-link\"><em>@ScholarRock</em></a><em> on X and on&nbsp;</em><a rel=\"noopener noreferrer\" href=\"https://www.linkedin.com/company/scholar-rock\" class=\"postings-link\"><em>LinkedIn</em></a><em>.</em></div>\n<div>&nbsp;</div>\n<div><strong style=\"font-size: 18px;\">Summary of Position:</strong></div><div><br></div><div><span style=\"font-size: 11pt;\">The Sr. Medical Director, Drug Safety &amp; Pharmacovigilance is a key position within the company and safety department, with significant impact on the development and life cycle of drug development projects. Responsible for providing safety strategy, expertise, and guidance, pre- and post-approval for assigned products, the Sr. Medical Director will drive the proactive implementation of risk management initiatives in accordance with global regulatory requirements. Core responsibilities will encompass continuous and efficient evaluation of safety data, perform signal detection, evaluation and assessment and management of the safety profile of the compound. In addition, the position will work closely with cross functional teams and Departments for achieving project goals, within timelines &amp; with high quality.</span></div>","id":"0f1cee85-bf7b-4669-9d4c-10f9442f2efc","lists":[{"text":"Position Responsibilities: ","content":"\n<li>Lead and support development of pharmacovigilance strategies for products within Therapeutic area, to ensure compliance with&nbsp;corporate clinical development and commercial goals.</li>\n<li>Oversight and conducting of signal detection activities include monitoring, evaluation, interpretation, management and&nbsp;communication of safety information.</li>\n<li>Responsible for oversight and conduct of Product Safety Committee (PSC) meeting(s) to evaluate risk-benefit for the&nbsp;compounds with support from cross-functional teams. Escalate and present safety issues to&nbsp;the Executive Safety Committee.</li>\n<li>Medical safety review including causality assessment of all available safety data generated from various&nbsp;sources (e.g. pre-clinical, clinical trial data, post-marketing and literature) throughout the development&nbsp;process for assigned compounds/projects.</li>\n<li>Provides medical expert safety review input into all critical documents for products in clinical&nbsp;development (e.g., INDs/NDA/BLA submissions, protocols and amendments, ICFs, IBs, and clinical&nbsp;research reports (CSR))</li>\n<li>Oversight of aggregate reports and signal evaluation reports for assigned projects.</li>\n<li>Responsible for the Clinical content of responses to inquiries from regulatory authorities related to&nbsp;Safety topics.</li>\n<li>Provide leadership and support to Contract Research Organization (CRO) staff to ensure overall&nbsp;delivery of services. Ensures vendor oversight of outsourced Medical activities, as applicable.</li>\n<li>Oversee and collaborate with internal safety scientists within TA</li>\n<li>Assist with the writing and development of SOPs as required to ensure compliance to regulations and local laws.</li>\n<li>Lead high quality planning and execution of external meetings and internal stakeholder meetings (e.g., DMCs, Vendor oversight meetings, etc.)</li>\n<li>Demonstrated ability to build effective working relationships, influence, negotiate, and drive organizational engagement. Ability to be flexible and adapt quickly to the changing needs of the organization.</li>\n<li>Support process improvement and functional training at departmental &amp; company level</li>\n<li>Ensure that the highest quality, ethical &amp; professional values are demonstrated in all aspects of work.</li>\n<li>Ensures compliance with corporate policies and procedures, as well as all related healthcare laws and regulations</li>\n"},{"text":"Candidate Requirements: ","content":"\n<li>MD or MBBS or MD-PhD or equivalent medical degree</li>\n<li>5 or more years of pharmaceutical experience in Drug Safety &amp; Pharmacovigilance.</li>\n<li>Strong understanding of pharmacovigilance regulations in the US and EU.</li>\n<li>Experience in supporting drug safety activities in registrational clinical studies</li>\n<li>High level of medical competence, with an ability to balance this with industry standards to achieve business goals</li>\n<li>Demonstrated skills in scientific analysis and reasoning.</li>\n<li>Sound knowledge of overall drug development process from discovery to registration and post marketing requirements &amp; surveillance.</li>\n<li>Prior IND, as well as NDA/BLA (filing/submission) and other regulatory interaction experience is highly desirable</li>\n<li>Strong track record of delivering results through effective team and peer leadership in matrix</li>\n<li>Excellent leadership &amp; organizational skills, analytical skills, presentation skills, and strong experience in translating important data into clinical strategies.</li>\n"}],"salaryRange":{"min":280000,"max":420000,"currency":"USD","interval":"per-year-salary"},"text":"Sr. Medical Director, Drug Safety & Pharmacovigilance","country":"US","workplaceType":"onsite","opening":"<div><em>Scholar Rock is a late-stage <span data-ogsc=\"red\">global&nbsp;</span>biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity.&nbsp;Scholar Rock&nbsp;works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at </em><a class=\"postings-link\" href=\"http://www.scholarrock.com/\" target=\"_blank\" rel=\"noopener noreferrer\"><em>ScholarRock.com</em></a><em> and follow </em><a class=\"postings-link\" href=\"http://www.twitter.com/scholarrock\" target=\"_blank\" rel=\"noopener noreferrer\"><em>@ScholarRock</em></a><em> on X and on&nbsp;</em><a class=\"postings-link\" href=\"https://www.linkedin.com/company/scholar-rock\" target=\"_blank\" rel=\"noopener noreferrer\"><em>LinkedIn</em></a><em>.</em></div>\n<div>&nbsp;</div>\n<div><strong style=\"font-size: 18px;\">Summary of Position:</strong></div>","openingPlain":"Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at ScholarRock.com and follow @ScholarRock on X and on LinkedIn.\n \nSummary of Position:\n","descriptionBody":"<div><span style=\"font-size: 11pt;\">The Sr. Medical Director, Drug Safety &amp; Pharmacovigilance is a key position within the company and safety department, with significant impact on the development and life cycle of drug development projects. Responsible for providing safety strategy, expertise, and guidance, pre- and post-approval for assigned products, the Sr. Medical Director will drive the proactive implementation of risk management initiatives in accordance with global regulatory requirements. Core responsibilities will encompass continuous and efficient evaluation of safety data, perform signal detection, evaluation and assessment and management of the safety profile of the compound. In addition, the position will work closely with cross functional teams and Departments for achieving project goals, within timelines &amp; with high quality.</span></div>","descriptionBodyPlain":"The Sr. Medical Director, Drug Safety & Pharmacovigilance is a key position within the company and safety department, with significant impact on the development and life cycle of drug development projects. Responsible for providing safety strategy, expertise, and guidance, pre- and post-approval for assigned products, the Sr. Medical Director will drive the proactive implementation of risk management initiatives in accordance with global regulatory requirements. Core responsibilities will encompass continuous and efficient evaluation of safety data, perform signal detection, evaluation and assessment and management of the safety profile of the compound. In addition, the position will work closely with cross functional teams and Departments for achieving project goals, within timelines & with high quality.\n","hostedUrl":"https://jobs.lever.co/scholarrock/0f1cee85-bf7b-4669-9d4c-10f9442f2efc","applyUrl":"https://jobs.lever.co/scholarrock/0f1cee85-bf7b-4669-9d4c-10f9442f2efc/apply"},{"additionalPlain":"Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. \n","additional":"<div><em>Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees</em>.&nbsp;</div>","categories":{"department":"Development","location":"Cambridge, MA","team":"Quality Assurance","allLocations":["Cambridge, MA"]},"createdAt":1787774966095,"descriptionPlain":"Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at ScholarRock.com and follow @ScholarRock on X and on LinkedIn.\n \nSummary of Position:\n\n\nScholar Rock is seeking an experienced and motivated Senior Director, Head of Clinical Quality Assurance to provide strategic and operational leadership for Good Clinical Practice (GCP) quality across the company’s biologics clinical development portfolio. Reporting to the Head of Global Quality, this role will serve as the senior Clinical QA leader and trusted partner to Clinical Operations, Clinical Development, Regulatory Affairs, Pharmacovigilance, Biometrics, Data Management, and external clinical service providers. The position is accountable for clinical quality strategy, GCP quality systems, clinical quality risk management, CRO and vendor oversight, audit strategy, inspection readiness, quality metrics, and the maturation of fit-for-purpose processes that embed quality by design across the clinical trial lifecycle.\n","description":"<div><em>Scholar Rock is a late-stage <span data-ogsc=\"red\">global&nbsp;</span>biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity.&nbsp;Scholar Rock&nbsp;works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at </em><a rel=\"noopener noreferrer\" href=\"http://www.scholarrock.com/\" class=\"postings-link\"><em>ScholarRock.com</em></a><em> and follow </em><a rel=\"noopener noreferrer\" href=\"http://www.twitter.com/scholarrock\" class=\"postings-link\"><em>@ScholarRock</em></a><em> on X and on&nbsp;</em><a rel=\"noopener noreferrer\" href=\"https://www.linkedin.com/company/scholar-rock\" class=\"postings-link\"><em>LinkedIn</em></a><em>.</em></div>\n<div>&nbsp;</div>\n<div><strong style=\"font-size: 18px;\">Summary of Position:</strong></div><div><br></div><div>\n<p>Scholar Rock is seeking an experienced and motivated Senior Director, Head of Clinical Quality Assurance to provide strategic and operational leadership for Good Clinical Practice (GCP) quality across the company’s biologics clinical development portfolio. Reporting to the Head of Global Quality, this role will serve as the senior Clinical QA leader and trusted partner to Clinical Operations, Clinical Development, Regulatory Affairs, Pharmacovigilance, Biometrics, Data Management, and external clinical service providers. The position is accountable for clinical quality strategy, GCP quality systems, clinical quality risk management, CRO and vendor oversight, audit strategy, inspection readiness, quality metrics, and the maturation of fit-for-purpose processes that embed quality by design across the clinical trial lifecycle.</p>\n</div>","id":"7430975a-df1f-4947-9f37-58d136868656","lists":[{"text":"Position Responsibilities: ","content":"<div>\n\n<li>Lead the Clinical Quality Assurance function, providing strategic direction and operational oversight for GCP quality across Scholar Rock-sponsored clinical trials, with a focus on biologics development programs.</li>\n<li>Serve as the senior GCP Quality partner to Clinical Operations, Clinical Development, Regulatory Affairs, Pharmacovigilance, Biometrics, Data Management, and other cross-functional stakeholders.</li>\n<li>Define, implement, and continuously mature the clinical quality strategy, governance model, and GCP quality management processes aligned with global regulatory expectations and clinical development priorities.</li>\n<li>Provide quality oversight for global clinical trials, including protocol compliance, informed consent processes, investigator site oversight, trial master file quality, data integrity, safety reporting interfaces, and clinical study documentation.</li>\n<li>Establish and execute a risk-based GCP audit program, including audits of investigator sites, CROs, vendors, clinical systems, TMF processes, and key internal clinical trial activities.</li>\n<li>Lead GCP inspection readiness activities and support preparation, conduct, response development, and follow-up for FDA, EMA, PMDA, and other health authority inspections.</li>\n<li>Provide oversight of GCP deviations, serious breaches, audit observations, inspection findings, CAPAs, and quality issues to ensure timely investigation, appropriate root cause analysis, effective corrective actions, and sustainable remediation.</li>\n<li>Oversee CRO and clinical vendor quality governance, including qualification, risk assessment, quality agreements where applicable, performance metrics, issue escalation, and continuous improvement.</li>\n<li>Partner with clinical and regulatory teams to proactively identify and mitigate quality risks associated with study design, trial execution, vendor performance, data integrity, patient safety, protocol deviations, and submission readiness.</li>\n<li>Develop and monitor GCP quality metrics, dashboards, and trend reports to support proactive risk management, governance discussions, and executive-level quality visibility.</li>\n<li>Author, review, and approve GCP-related SOPs, policies, quality plans, audit reports, CAPA plans, inspection materials, and other controlled documents as appropriate.</li>\n<li>Build, lead, and develop a fit-for-purpose Clinical QA function appropriate for a fast-paced, outsourced biotech operating model.</li>\n<li>Champion a culture of quality, accountability, patient safety, data integrity, transparency, and continuous improvement across internal teams and external partners.</li>\n\n</div>"},{"text":"Candidate Requirements:","content":"<div>\n\n<li>BS/MS degree in a scientific, healthcare, or related discipline; advanced degree preferred.</li>\n<li>15+ years of experience in the pharmaceutical/biotech industry, including significant experience in Clinical Quality Assurance, Clinical Operations, clinical development, or related GCP compliance roles.</li>\n<li>10+ years of hands-on GCP quality experience, including leadership of global clinical quality programs and oversight of Phase I–III clinical trials.</li>\n<li>Deep knowledge of ICH-GCP, ICH E6(R3), FDA, EMA, PMDA, and other global clinical trial regulations and expectations.</li>\n<li>Experience supporting biologics clinical development programs; late-stage development, registration-enabling studies, and inspection readiness experience strongly preferred.</li>\n<li>Demonstrated experience leading or supporting regulatory inspections, including inspection preparation, hosting, response development, CAPA management, and follow-up commitments.</li>\n<li>Strong experience with CRO and clinical vendor oversight, investigator site audits, TMF quality, clinical systems, data integrity, risk-based quality management, and quality issue escalation.</li>\n<li>Proven ability to design and mature fit-for-purpose GCP quality systems, SOPs, audit programs, quality metrics, governance forums, and inspection readiness frameworks in an outsourced biotech model.</li>\n<li>Strong judgment, executive presence, technical writing capability, and the ability to influence cross-functional leaders and external partners.</li>\n<li>Highly proactive, decisive, and capable of balancing strategic leadership with hands-on execution in a fast-paced environment.</li>\n<li>Engaged leader committed to building culture, mentoring talent, and developing scalable Clinical QA capabilities.</li>\n\n</div>"}],"salaryRange":{"min":270000,"max":300000,"currency":"USD","interval":"per-year-salary"},"text":"Title: Sr. Director, Head of Clinical Quality Assurance","country":"US","workplaceType":"hybrid","opening":"<div><em>Scholar Rock is a late-stage <span data-ogsc=\"red\">global&nbsp;</span>biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity.&nbsp;Scholar Rock&nbsp;works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at </em><a class=\"postings-link\" href=\"http://www.scholarrock.com/\" target=\"_blank\" rel=\"noopener noreferrer\"><em>ScholarRock.com</em></a><em> and follow </em><a class=\"postings-link\" href=\"http://www.twitter.com/scholarrock\" target=\"_blank\" rel=\"noopener noreferrer\"><em>@ScholarRock</em></a><em> on X and on&nbsp;</em><a class=\"postings-link\" href=\"https://www.linkedin.com/company/scholar-rock\" target=\"_blank\" rel=\"noopener noreferrer\"><em>LinkedIn</em></a><em>.</em></div>\n<div>&nbsp;</div>\n<div><strong style=\"font-size: 18px;\">Summary of Position:</strong></div>","openingPlain":"Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at ScholarRock.com and follow @ScholarRock on X and on LinkedIn.\n \nSummary of Position:\n","descriptionBody":"<div>\n<p>Scholar Rock is seeking an experienced and motivated Senior Director, Head of Clinical Quality Assurance to provide strategic and operational leadership for Good Clinical Practice (GCP) quality across the company&rsquo;s biologics clinical development portfolio. Reporting to the Head of Global Quality, this role will serve as the senior Clinical QA leader and trusted partner to Clinical Operations, Clinical Development, Regulatory Affairs, Pharmacovigilance, Biometrics, Data Management, and external clinical service providers. The position is accountable for clinical quality strategy, GCP quality systems, clinical quality risk management, CRO and vendor oversight, audit strategy, inspection readiness, quality metrics, and the maturation of fit-for-purpose processes that embed quality by design across the clinical trial lifecycle.</p>\n</div>","descriptionBodyPlain":"Scholar Rock is seeking an experienced and motivated Senior Director, Head of Clinical Quality Assurance to provide strategic and operational leadership for Good Clinical Practice (GCP) quality across the company’s biologics clinical development portfolio. Reporting to the Head of Global Quality, this role will serve as the senior Clinical QA leader and trusted partner to Clinical Operations, Clinical Development, Regulatory Affairs, Pharmacovigilance, Biometrics, Data Management, and external clinical service providers. The position is accountable for clinical quality strategy, GCP quality systems, clinical quality risk management, CRO and vendor oversight, audit strategy, inspection readiness, quality metrics, and the maturation of fit-for-purpose processes that embed quality by design across the clinical trial lifecycle.\n","hostedUrl":"https://jobs.lever.co/scholarrock/7430975a-df1f-4947-9f37-58d136868656","applyUrl":"https://jobs.lever.co/scholarrock/7430975a-df1f-4947-9f37-58d136868656/apply"},{"additionalPlain":"Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. \n","additional":"<div><em>Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees</em>.&nbsp;</div>","categories":{"commitment":"Full-Time","department":"G&A","location":"Cambridge, MA","team":"Legal","allLocations":["Cambridge, MA"]},"createdAt":1784059503285,"descriptionPlain":"Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at ScholarRock.com and follow @ScholarRock on X and on LinkedIn.\n \nSummary of Position:\n\n\nScholar Rock is seeking an experienced biopharmaceutical attorney with rare disease product launch experience to serve as VP, Commercial Legal Counsel.  The position reports to the General Counsel & Corporate Secretary and is a key partner to the U.S. commercial and medical affairs organization, responsible for providing strategic legal guidance related to Scholar Rock’s planned commercialization activities.  \n\n","description":"<div><em>Scholar Rock is a late-stage <span data-ogsc=\"red\">global&nbsp;</span>biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity.&nbsp;Scholar Rock&nbsp;works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at </em><a rel=\"noopener noreferrer\" href=\"http://www.scholarrock.com/\" class=\"postings-link\"><em>ScholarRock.com</em></a><em> and follow </em><a rel=\"noopener noreferrer\" href=\"http://www.twitter.com/scholarrock\" class=\"postings-link\"><em>@ScholarRock</em></a><em> on X and on&nbsp;</em><a rel=\"noopener noreferrer\" href=\"https://www.linkedin.com/company/scholar-rock\" class=\"postings-link\"><em>LinkedIn</em></a><em>.</em></div>\n<div>&nbsp;</div>\n<div><strong style=\"font-size: 18px;\">Summary of Position:</strong></div><div><br></div><div>Scholar Rock is seeking an experienced biopharmaceutical attorney with rare disease product launch experience to serve as VP, Commercial Legal Counsel.&nbsp; The position reports to the General Counsel &amp; Corporate Secretary and is a key partner to the U.S. commercial and medical affairs organization, responsible for providing strategic legal guidance related to Scholar Rock’s planned commercialization activities.&nbsp; <br><br></div>","id":"e38c9965-3691-4001-aa93-19a680d90298","lists":[{"text":"Position Responsibilities","content":"<div>\n<ul type=\"disc\">\n<li>Provide legal advice on a wide range of commercialization issues with broad enterprise impact.</li>\n<li>Strategic legal partner for U.S. commercial and medical affairs organization.</li>\n<li>Advise business on advertising and promotional messaging, materials and activities, including serving on review committees to review and advise on promotional, medical, scientific exchange, and educational materials.</li>\n<li>Review and advise on interactions with external stakeholders, including patients, physicians, payors and patient advocacy groups.</li>\n<li>Provide strategic legal advice related to patient support programs, patient hubs, market access, pricing, reimbursement, and distribution channels and manage commercial contracting.</li>\n<li>Collaborate with compliance to ensure commercialization activities conducted compliantly, in accordance with applicable laws and company policies.</li>\n<li>Monitor healthcare regulatory laws and emerging legal trends, including FDCA and related regulations, fraud and abuse laws and guidance (Anti-Kickback Statute, False Claims Act, OIG guidance and advisory opinions), and assess their impact on Scholar Rock.</li>\n<li>Work closely and collaboratively with broader legal team on legal initiatives.</li>\n<li>Provide company-wide education/trainings on healthcare regulatory laws and emerging trends.</li>\n<li>Develop and mentor legal colleagues to help build a successful legal team.</li>\n\n</ul></div>"},{"text":"Candidate Requirements","content":"<div>\n<ul type=\"disc\">\n<li>Juris Doctorate (J.D.) from a fully accredited law school.</li>\n<li>Admission to the Massachusetts bar.</li>\n<li>15+ years of legal experience, with leadership experience at a commercial stage biopharma company preferred.</li>\n<li>Deep familiarity with healthcare compliance laws, including FDA advertising and promotion compliance.</li>\n<li>Exceptional executive-level written and verbal communication skills with ability to convey complex legal risks in clear, business‑centric terms.</li>\n<li>Experience supporting rare disease product launches.</li>\n<li>Ability to maintain confidentiality and operate with high ethical standards and professionalism.</li>\n<li>Exceptional interpersonal skills and ability to work collaboratively in a fast-paced global environment.</li>\n<li>Hybrid schedule (in-office required for a portion of the week).</li>\n\n</ul></div>"}],"salaryRange":{"min":325000,"max":400000,"currency":"USD","interval":"per-year-salary"},"text":"Vice President, Commercial Legal Counsel","country":"US","workplaceType":"onsite","opening":"<div><em>Scholar Rock is a late-stage <span data-ogsc=\"red\">global&nbsp;</span>biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity.&nbsp;Scholar Rock&nbsp;works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at </em><a class=\"postings-link\" href=\"http://www.scholarrock.com/\" target=\"_blank\" rel=\"noopener noreferrer\"><em>ScholarRock.com</em></a><em> and follow </em><a class=\"postings-link\" href=\"http://www.twitter.com/scholarrock\" target=\"_blank\" rel=\"noopener noreferrer\"><em>@ScholarRock</em></a><em> on X and on&nbsp;</em><a class=\"postings-link\" href=\"https://www.linkedin.com/company/scholar-rock\" target=\"_blank\" rel=\"noopener noreferrer\"><em>LinkedIn</em></a><em>.</em></div>\n<div>&nbsp;</div>\n<div><strong style=\"font-size: 18px;\">Summary of Position:</strong></div>","openingPlain":"Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at ScholarRock.com and follow @ScholarRock on X and on LinkedIn.\n \nSummary of Position:\n","descriptionBody":"<div>Scholar Rock is seeking an experienced biopharmaceutical attorney with rare disease product launch experience to serve as VP, Commercial Legal Counsel.&nbsp; The position reports to the General Counsel &amp; Corporate Secretary and is a key partner to the U.S. commercial and medical affairs organization, responsible for providing strategic legal guidance related to Scholar Rock&rsquo;s planned commercialization activities.&nbsp; <br><br></div>","descriptionBodyPlain":"Scholar Rock is seeking an experienced biopharmaceutical attorney with rare disease product launch experience to serve as VP, Commercial Legal Counsel.  The position reports to the General Counsel & Corporate Secretary and is a key partner to the U.S. commercial and medical affairs organization, responsible for providing strategic legal guidance related to Scholar Rock’s planned commercialization activities.  \n\n","hostedUrl":"https://jobs.lever.co/scholarrock/e38c9965-3691-4001-aa93-19a680d90298","applyUrl":"https://jobs.lever.co/scholarrock/e38c9965-3691-4001-aa93-19a680d90298/apply"}]