[{"additional":"","additionalPlain":"","categories":{"commitment":"Full-Time","department":"4112 - Bioanalytical Services","location":"Fehraltorf (Zurich), Switzerland","team":"4112 - Bioanalytical Services","allLocations":["Fehraltorf (Zurich), Switzerland"]},"createdAt":1786435398020,"descriptionPlain":"Celerion is one of the world's leading bioanalytical contract research organizations and has been supporting pharmaceutical and biotech drug development programs around the world for more than 40 years.\n \nDue to the steady growth of our company and to strengthen our bioanalytical laboratory in Fehraltorf / Zurich, we are looking for a\n \n(Liquid Handling) Automation Specialist (80 – 100 %)\n \nYou will convert bioanalytical assay workflows defined by R&D into robust, documented and supportable robotic routines.\nYour primary tasks would consist of programming using the VENUS and EVOware software, as well as regularly assessing our robots’ performance.\nAs part of our team, you will become a key component to successfully use the liquid handling robots to improve the performance and throughput of our assays, and you will help Celerion maintain its competitive position in the market\n \nYour Profile\nBachelor’s or Master’s degree in a life-science discipline (e.g. Biology, Chemistry, Biotechnology). (Please note: this role targets a life-science background; engineering degrees are not the intended profile)\nSolid understanding of immunoassays and/or chromatographic methods\nAt least 1 year demonstrated hands-on experience programming Hamilton liquid-handling robots using VENUS software to support automated workflows in a regulated laboratory environment \nGood written and spoken German is beneficial\nHighly collaborative and service-oriented mindset\nStrong problem-solving skills with a hands-on approach\nStructured, detail-oriented, and quality-focused\nAble to balance development work with operational support\nExperience with general-purpose programming languages such as Python, VB or SQL is beneficial but not required; proven Hamilton VENUS method-programming experience is essential.\nWe Offer You\n \nA technically specialized role in the interface of bioanalytical science, automation and regulated laboratory operations, with direct impact on throughput, standardization and reliability Structured onboarding and internal training programme.\nOpportunity to contribute and shape the continuous development of Celerion’s automation capabilities.\nModern infrastructure and work environment\nWork-life balance: flexible working hours (Monday to Friday, no weekends, no shift work), 5 weeks of vacation\nFinancial benefits: equal pay regardless of gender, excellent social benefits, and access to REKA vouchers\n \nDoes this sound like the right opportunity for you? We look forward to receiving your complete application, including your CV, references, diplomas, and other relevant documents.\n \nAdditional information can be found on our website:\n https://www.celerion.com/careers\n \n \n","description":"\n
Celerion is one of the world's leading bioanalytical contract research organizations and has been supporting pharmaceutical and biotech drug development programs around the world for more than 40 years.
\n
\n
Due to the steady growth of our company and to strengthen our bioanalytical laboratory in Fehraltorf / Zurich, we are looking for a
\n
\n
(Liquid Handling) Automation Specialist (80 – 100 %)
\n
\n
\n- You will convert bioanalytical assay workflows defined by R&D into robust, documented and supportable robotic routines.
\n- Your primary tasks would consist of programming using the VENUS and EVOware software, as well as regularly assessing our robots’ performance.
\n- As part of our team, you will become a key component to successfully use the liquid handling robots to improve the performance and throughput of our assays, and you will help Celerion maintain its competitive position in the market
\n
\n
\n
Your Profile
\n
\n- Bachelor’s or Master’s degree in a life-science discipline (e.g. Biology, Chemistry, Biotechnology). (Please note: this role targets a life-science background; engineering degrees are not the intended profile)
\n- Solid understanding of immunoassays and/or chromatographic methods
\n- At least 1 year demonstrated hands-on experience programming Hamilton liquid-handling robots using VENUS software to support automated workflows in a regulated laboratory environment
\n- Good written and spoken German is beneficial
\n
\n
\n- Highly collaborative and service-oriented mindset
\n- Strong problem-solving skills with a hands-on approach
\n- Structured, detail-oriented, and quality-focused
\n- Able to balance development work with operational support
\n
\n
Experience with general-purpose programming languages such as Python, VB or SQL is beneficial but not required; proven Hamilton VENUS method-programming experience is essential.
\n
We Offer You
\n
\n
\n- A technically specialized role in the interface of bioanalytical science, automation and regulated laboratory operations, with direct impact on throughput, standardization and reliability Structured onboarding and internal training programme.
\n- Opportunity to contribute and shape the continuous development of Celerion’s automation capabilities.
\n- Modern infrastructure and work environment
\n- Work-life balance: flexible working hours (Monday to Friday, no weekends, no shift work), 5 weeks of vacation
\n- Financial benefits: equal pay regardless of gender, excellent social benefits, and access to REKA vouchers
\n
\n
\n
Does this sound like the right opportunity for you? We look forward to receiving your complete application, including your CV, references, diplomas, and other relevant documents.
\n
\n
Additional information can be found on our website:
\n
https://www.celerion.com/careers
\n
\n
","id":"4daa3170-60fc-4fd6-a932-11335a05c9f2","lists":[],"text":"(Liquid Handling) Automation Specialist (80 – 100 %)","country":"CH","workplaceType":"onsite","opening":"","openingPlain":"","descriptionBody":"\n
Celerion is one of the world's leading bioanalytical contract research organizations and has been supporting pharmaceutical and biotech drug development programs around the world for more than 40 years.
\n
\n
Due to the steady growth of our company and to strengthen our bioanalytical laboratory in Fehraltorf / Zurich, we are looking for a
\n
\n
(Liquid Handling) Automation Specialist (80 – 100 %)
\n
\n
\n- You will convert bioanalytical assay workflows defined by R&D into robust, documented and supportable robotic routines.
\n- Your primary tasks would consist of programming using the VENUS and EVOware software, as well as regularly assessing our robots’ performance.
\n- As part of our team, you will become a key component to successfully use the liquid handling robots to improve the performance and throughput of our assays, and you will help Celerion maintain its competitive position in the market
\n
\n
\n
Your Profile
\n
\n- Bachelor’s or Master’s degree in a life-science discipline (e.g. Biology, Chemistry, Biotechnology). (Please note: this role targets a life-science background; engineering degrees are not the intended profile)
\n- Solid understanding of immunoassays and/or chromatographic methods
\n- At least 1 year demonstrated hands-on experience programming Hamilton liquid-handling robots using VENUS software to support automated workflows in a regulated laboratory environment
\n- Good written and spoken German is beneficial
\n
\n
\n- Highly collaborative and service-oriented mindset
\n- Strong problem-solving skills with a hands-on approach
\n- Structured, detail-oriented, and quality-focused
\n- Able to balance development work with operational support
\n
\n
Experience with general-purpose programming languages such as Python, VB or SQL is beneficial but not required; proven Hamilton VENUS method-programming experience is essential.
\n
We Offer You
\n
\n
\n- A technically specialized role in the interface of bioanalytical science, automation and regulated laboratory operations, with direct impact on throughput, standardization and reliability Structured onboarding and internal training programme.
\n- Opportunity to contribute and shape the continuous development of Celerion’s automation capabilities.
\n- Modern infrastructure and work environment
\n- Work-life balance: flexible working hours (Monday to Friday, no weekends, no shift work), 5 weeks of vacation
\n- Financial benefits: equal pay regardless of gender, excellent social benefits, and access to REKA vouchers
\n
\n
\n
Does this sound like the right opportunity for you? We look forward to receiving your complete application, including your CV, references, diplomas, and other relevant documents.
\n
\n
Additional information can be found on our website:
\n
https://www.celerion.com/careers
\n
\n
","descriptionBodyPlain":"Celerion is one of the world's leading bioanalytical contract research organizations and has been supporting pharmaceutical and biotech drug development programs around the world for more than 40 years.\n \nDue to the steady growth of our company and to strengthen our bioanalytical laboratory in Fehraltorf / Zurich, we are looking for a\n \n(Liquid Handling) Automation Specialist (80 – 100 %)\n \nYou will convert bioanalytical assay workflows defined by R&D into robust, documented and supportable robotic routines.\nYour primary tasks would consist of programming using the VENUS and EVOware software, as well as regularly assessing our robots’ performance.\nAs part of our team, you will become a key component to successfully use the liquid handling robots to improve the performance and throughput of our assays, and you will help Celerion maintain its competitive position in the market\n \nYour Profile\nBachelor’s or Master’s degree in a life-science discipline (e.g. Biology, Chemistry, Biotechnology). (Please note: this role targets a life-science background; engineering degrees are not the intended profile)\nSolid understanding of immunoassays and/or chromatographic methods\nAt least 1 year demonstrated hands-on experience programming Hamilton liquid-handling robots using VENUS software to support automated workflows in a regulated laboratory environment \nGood written and spoken German is beneficial\nHighly collaborative and service-oriented mindset\nStrong problem-solving skills with a hands-on approach\nStructured, detail-oriented, and quality-focused\nAble to balance development work with operational support\nExperience with general-purpose programming languages such as Python, VB or SQL is beneficial but not required; proven Hamilton VENUS method-programming experience is essential.\nWe Offer You\n \nA technically specialized role in the interface of bioanalytical science, automation and regulated laboratory operations, with direct impact on throughput, standardization and reliability Structured onboarding and internal training programme.\nOpportunity to contribute and shape the continuous development of Celerion’s automation capabilities.\nModern infrastructure and work environment\nWork-life balance: flexible working hours (Monday to Friday, no weekends, no shift work), 5 weeks of vacation\nFinancial benefits: equal pay regardless of gender, excellent social benefits, and access to REKA vouchers\n \nDoes this sound like the right opportunity for you? We look forward to receiving your complete application, including your CV, references, diplomas, and other relevant documents.\n \nAdditional information can be found on our website:\n https://www.celerion.com/careers\n \n \n","hostedUrl":"https://jobs.lever.co/celerion/4daa3170-60fc-4fd6-a932-11335a05c9f2","applyUrl":"https://jobs.lever.co/celerion/4daa3170-60fc-4fd6-a932-11335a05c9f2/apply"},{"additional":"","additionalPlain":"","categories":{"commitment":"Full-Time","department":"4112 - Bioanalytical Services","location":"Fehraltorf (Zurich), Switzerland","team":"4112 - Bioanalytical Services","allLocations":["Fehraltorf (Zurich), Switzerland"]},"createdAt":1782219033930,"descriptionPlain":"Shape the future of bioanalysis for innovative medicines\n \nCelerion is a leading global contract research organization (CRO) specializing in early clinical research and bioanalytical services. For more than 40 years, we have partnered with pharmaceutical and biotechnology companies worldwide to accelerate the development of new therapies and bring life-changing medicines to patients faster.\nTo support the continued growth of our Bioanalytical Laboratory in Fehraltorf (Zurich area), Switzerland, we are looking for a motivated and scientifically driven professional to join our Ligand Binding Services (LBS) team as a:\n \n(Senior) Bioanalytical Principal Investigator LBS / GLP Study Director (100%)\n \nIn this role, you will take scientific and operational ownership of regulated bioanalytical studies and method validations. You will serve as the primary client contact, lead study execution from planning through reporting, and play a key role in delivering high-quality data to support drug development programs worldwide.\n","description":"\n
Shape the future of bioanalysis for innovative medicines
\n
\n
Celerion is a leading global contract research organization (CRO) specializing in early clinical research and bioanalytical services. For more than 40 years, we have partnered with pharmaceutical and biotechnology companies worldwide to accelerate the development of new therapies and bring life-changing medicines to patients faster.
\n
To support the continued growth of our Bioanalytical Laboratory in Fehraltorf (Zurich area), Switzerland, we are looking for a motivated and scientifically driven professional to join our Ligand Binding Services (LBS) team as a:
\n
\n
(Senior) Bioanalytical Principal Investigator LBS / GLP Study Director (100%)
\n
\n
In this role, you will take scientific and operational ownership of regulated bioanalytical studies and method validations. You will serve as the primary client contact, lead study execution from planning through reporting, and play a key role in delivering high-quality data to support drug development programs worldwide.
\n
\n
Study Leadership & Scientific Oversight
\n
Lead and oversee GLP/GxP-compliant bioanalytical studies and method validations within the Ligand Binding Services (LBS) department.
\n
Act as Study Director and/or Principal Investigator with full responsibility for assigned studies or study phases.
\n
Develop and approve study plans, validation protocols, analytical reports and associated study documentation.
\n
Review, evaluate and approve analytical data to ensure scientific integrity and regulatory compliance.
\n
Ensure all study activities are conducted in accordance with applicable SOPs, regulatory requirements and client expectations.
\n
Client Management
\n
Serve as the primary scientific and operational contact for assigned clients.
\n
Provide regular project updates and maintain strong communication throughout the study lifecycle.
\n
Support client meetings, scientific discussions and audits as required.
\n
Operational Excellence
\n
Coordinate laboratory activities and ensure efficient study execution.
\n
Train, mentor and support assigned laboratory personnel.
\n
Contribute to process improvements and continuous enhancement of laboratory operations and quality standards.
\n
Support bioanalytical data management activities and documentation review processes.
\n
Additional Responsibilities for Senior-Level Candidates
\n
Lead complex or strategic client programs.
\n
Provide scientific mentoring and guidance to junior Principal Investigators and laboratory staff.
\n
Act as a subject matter expert for ligand-binding and cell-based assay technologies.
\n
Contribute to business development activities, client presentations and scientific initiatives.
\n
\n
Required Qualifications
\n
\n- Degree in Biochemistry, Biology, Chemistry or a related scientific discipline; PhD is advantageous.
\n- Minimum 2 years of experience in bioanalysis or quantitative analytical sciences.
\n- Hands-on experience with ligand-binding assays and/or cell-based assays.
\n- Experience working in a regulated environment (GLP, GCP, GMP and/or ISO standards).
\n- Strong analytical thinking and problem-solving skills.
\n- Excellent written and verbal communication skills in English.
\n- Ability to manage multiple projects while maintaining a high level of quality and attention to detail.
\n\n
\nPreferred Qualifications
\n\n- Previous experience as a Study Director, Principal Investigator or equivalent scientific leadership role.
\n- Knowledge of biomarker, pharmacokinetic (PK), immunogenicity (ADA) or biologics bioanalysis.
\n- Good German language skills.
\n- Experience working directly with pharmaceutical or biotechnology clients.
\n\n
\n
\n- The opportunity to lead scientifically challenging projects for global pharmaceutical and biotech clients.
\n- Exposure to innovative biologics, biomarkers and emerging therapeutic modalities.
\n- A collaborative, international and science-driven working environment.
\n- Structured onboarding and continuous professional development opportunities.
\n- Modern laboratories and state-of-the-art infrastructure.
\n- Flexible working hours and attractive employment conditions.
\n- The opportunity to grow your career within a globally recognized CRO.
\n- A workplace located near Zurich with easy access to excellent public transportation and recreational opportunities.
\n\n
\nWhy Join Celerion?
\nAt Celerion, you will contribute directly to the development of new medicines while working alongside highly skilled scientists in a dynamic and supportive environment. We value scientific excellence, teamwork, integrity and innovation, and we are committed to helping our employees grow and succeed.
\nCelerion is an equal opportunity employer. We welcome applications from candidates of all backgrounds and are committed to fostering an inclusive and diverse workplace.
\n
\nInterested?
\nWe look forward to receiving your application.
\nJoin us in advancing the development of tomorrow's medicines.
\n
\n
Shape the future of bioanalysis for innovative medicines
\n
\n
Celerion is a leading global contract research organization (CRO) specializing in early clinical research and bioanalytical services. For more than 40 years, we have partnered with pharmaceutical and biotechnology companies worldwide to accelerate the development of new therapies and bring life-changing medicines to patients faster.
\n
To support the continued growth of our Bioanalytical Laboratory in Fehraltorf (Zurich area), Switzerland, we are looking for a motivated and scientifically driven professional to join our Ligand Binding Services (LBS) team as a:
\n
\n
(Senior) Bioanalytical Principal Investigator LBS / GLP Study Director (100%)
\n
\n
In this role, you will take scientific and operational ownership of regulated bioanalytical studies and method validations. You will serve as the primary client contact, lead study execution from planning through reporting, and play a key role in delivering high-quality data to support drug development programs worldwide.
\n
Celerion Values: Integrity Trust Teamwork Respect
\n
\nCelerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.
\n
\n\n
Note: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as \"Not Junk\" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.
\n
\n
Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
We are seeking a full-time Bioanalytical Fee & Proposal Support professional to join our Bioanalytical Services team. In this role, you will support the development of scopes, budgets, and pricing for bioanalytical studies, working closely with Business Development, Operations, Finance, and Contracts teams.
\nThis position plays a key role in ensuring accurate, competitive, and compliant proposals while supporting the financial lifecycle of awarded studies—from forecasting through close-out.
\nProposal & Pricing Support
\n\n- Support study scoping and development of bioanalytical budgets and fee estimates.
\n- Prepare pricing materials for proposals, RFQs, bid grids, cost assumptions, and timelines.
\n- Assist with quotation and contract preparation, project number creation, and document tracking.
\n- Support change orders by evaluating scope changes and financial impacts.
\n- Maintain consistency and accuracy across pricing models, templates, and assumptions.
\n- Collaborate with cross-functional stakeholders to develop competitive pricing strategies.
\n
\nFinancial & Project Support
\n\n- Provide financial support for awarded bioanalytical projects, ensuring alignment between scope, budget, and actuals.
\n- Maintain project data in local and global systems with timely updates.
\n- Assist with weekly forecasting, variance tracking, and WIP monitoring.
\n- Support invoice preparation and allocation of pass-through costs.
\n- Partner with Finance and Contracts to ensure alignment between budgets, fees, and contractual terms.
\n- Assist with financial inquiries, adjustments, and project close-out activities.
\n
\nSystems & Process Improvement
\n\n- Support development and optimization of Smartsheet tools and pricing templates.
\n- Utilize AI and automation to improve efficiency and data accuracy.
\n- Identify opportunities for continuous improvement in proposal, pricing, and financial processes.
\n- Assist with ordering study-specific materials and supplies for the Bioanalytical department.
\n
\n
","id":"27555349-a788-4cb0-8347-8554b60f169a","lists":[{"text":"Requirements","content":"\n\n
Bachelor’s degree in Business, Finance, Accounting, Life Sciences, or a related field
(or equivalent combination of education and experience).\n
2–4 years of experience in proposal support, pricing, financial operations, or project coordination.\n
Experience supporting client-facing, project-based budgets and financial tracking.\n
Strong proficiency in Microsoft Excel (advanced formulas, analysis, templates).\n
Exceptional attention to detail and commitment to data accuracy.\n
Strong analytical, organizational, and problem-solving skills.\n
Ability to manage multiple priorities in a deadline-driven environment.\n
Effective written and verbal communication skills.\n\n
\n
\n
Preferred Qualifications
\n\n
Experience in bioanalytical services, clinical research, or life sciences.\n
Familiarity with Smartsheet or similar workflow/project management tools.\n
Exposure to RFQs, change orders, contracts, and quotations.\n\n
\n
Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
","openingPlain":"Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. \n","descriptionBody":"We are seeking a full-time Bioanalytical Fee & Proposal Support professional to join our Bioanalytical Services team. In this role, you will support the development of scopes, budgets, and pricing for bioanalytical studies, working closely with Business Development, Operations, Finance, and Contracts teams.
\nThis position plays a key role in ensuring accurate, competitive, and compliant proposals while supporting the financial lifecycle of awarded studies—from forecasting through close-out.
\nProposal & Pricing Support
\n\n- Support study scoping and development of bioanalytical budgets and fee estimates.
\n- Prepare pricing materials for proposals, RFQs, bid grids, cost assumptions, and timelines.
\n- Assist with quotation and contract preparation, project number creation, and document tracking.
\n- Support change orders by evaluating scope changes and financial impacts.
\n- Maintain consistency and accuracy across pricing models, templates, and assumptions.
\n- Collaborate with cross-functional stakeholders to develop competitive pricing strategies.
\n
\nFinancial & Project Support
\n\n- Provide financial support for awarded bioanalytical projects, ensuring alignment between scope, budget, and actuals.
\n- Maintain project data in local and global systems with timely updates.
\n- Assist with weekly forecasting, variance tracking, and WIP monitoring.
\n- Support invoice preparation and allocation of pass-through costs.
\n- Partner with Finance and Contracts to ensure alignment between budgets, fees, and contractual terms.
\n- Assist with financial inquiries, adjustments, and project close-out activities.
\n
\nSystems & Process Improvement
\n\n- Support development and optimization of Smartsheet tools and pricing templates.
\n- Utilize AI and automation to improve efficiency and data accuracy.
\n- Identify opportunities for continuous improvement in proposal, pricing, and financial processes.
\n- Assist with ordering study-specific materials and supplies for the Bioanalytical department.
\n
\n
","descriptionBodyPlain":"We are seeking a full-time Bioanalytical Fee & Proposal Support professional to join our Bioanalytical Services team. In this role, you will support the development of scopes, budgets, and pricing for bioanalytical studies, working closely with Business Development, Operations, Finance, and Contracts teams.\nThis position plays a key role in ensuring accurate, competitive, and compliant proposals while supporting the financial lifecycle of awarded studies—from forecasting through close-out.\nProposal & Pricing Support\nSupport study scoping and development of bioanalytical budgets and fee estimates.\nPrepare pricing materials for proposals, RFQs, bid grids, cost assumptions, and timelines.\nAssist with quotation and contract preparation, project number creation, and document tracking.\nSupport change orders by evaluating scope changes and financial impacts.\nMaintain consistency and accuracy across pricing models, templates, and assumptions.\nCollaborate with cross-functional stakeholders to develop competitive pricing strategies.\nFinancial & Project Support\nProvide financial support for awarded bioanalytical projects, ensuring alignment between scope, budget, and actuals.\nMaintain project data in local and global systems with timely updates.\nAssist with weekly forecasting, variance tracking, and WIP monitoring.\nSupport invoice preparation and allocation of pass-through costs.\nPartner with Finance and Contracts to ensure alignment between budgets, fees, and contractual terms.\nAssist with financial inquiries, adjustments, and project close-out activities.\nSystems & Process Improvement\nSupport development and optimization of Smartsheet tools and pricing templates.\nUtilize AI and automation to improve efficiency and data accuracy.\nIdentify opportunities for continuous improvement in proposal, pricing, and financial processes.\nAssist with ordering study-specific materials and supplies for the Bioanalytical department.\n \n","hostedUrl":"https://jobs.lever.co/celerion/27555349-a788-4cb0-8347-8554b60f169a","applyUrl":"https://jobs.lever.co/celerion/27555349-a788-4cb0-8347-8554b60f169a/apply"},{"additionalPlain":"Celerion Values: Integrity Trust Teamwork Respect\n \nCelerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.\n \nNote: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as \"Not Junk\" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.\n \n","additional":"Celerion Values: Integrity Trust Teamwork Respect
\n
\nCelerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.
\n
\n\n
Note: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as \"Not Junk\" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.
\n
\n
Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
We are seeking a full-time Bioanalytical Fee & Proposal Support professional to join our Bioanalytical Services team. In this role, you will support the development of scopes, budgets, and pricing for bioanalytical studies, working closely with Business Development, Operations, Finance, and Contracts teams.
\nThis position plays a key role in ensuring accurate, competitive, and compliant proposals while supporting the financial lifecycle of awarded studies—from forecasting through close-out.
\nProposal & Pricing Support
\n\n- Support study scoping and development of bioanalytical budgets and fee estimates.
\n- Prepare pricing materials for proposals, RFQs, bid grids, cost assumptions, and timelines.
\n- Assist with quotation and contract preparation, project number creation, and document tracking.
\n- Support change orders by evaluating scope changes and financial impacts.
\n- Maintain consistency and accuracy across pricing models, templates, and assumptions.
\n- Collaborate with cross-functional stakeholders to develop competitive pricing strategies.
\n
\nFinancial & Project Support
\n\n- Provide financial support for awarded bioanalytical projects, ensuring alignment between scope, budget, and actuals.
\n- Maintain project data in local and global systems with timely updates.
\n- Assist with weekly forecasting, variance tracking, and WIP monitoring.
\n- Support invoice preparation and allocation of pass-through costs.
\n- Partner with Finance and Contracts to ensure alignment between budgets, fees, and contractual terms.
\n- Assist with financial inquiries, adjustments, and project close-out activities.
\n
\nSystems & Process Improvement
\n\n- Support development and optimization of Smartsheet tools and pricing templates.
\n- Utilize AI and automation to improve efficiency and data accuracy.
\n- Identify opportunities for continuous improvement in proposal, pricing, and financial processes.
\n- Assist with ordering study-specific materials and supplies for the Bioanalytical department.
\n
\n
","id":"9d79cb5f-7597-4454-92a1-67eae3f714d3","lists":[{"text":"Requirements","content":"\n\n
Bachelor’s degree in Business, Finance, Accounting, Life Sciences, or a related field
(or equivalent combination of education and experience).\n
2–4 years of experience in proposal support, pricing, financial operations, or project coordination.\n
Experience supporting client-facing, project-based budgets and financial tracking.\n
Strong proficiency in Microsoft Excel (advanced formulas, analysis, templates).\n
Exceptional attention to detail and commitment to data accuracy.\n
Strong analytical, organizational, and problem-solving skills.\n
Ability to manage multiple priorities in a deadline-driven environment.\n
Effective written and verbal communication skills.\n\n
\n
\n
Preferred Qualifications
\n\n
Experience in bioanalytical services, clinical research, or life sciences.\n
Familiarity with Smartsheet or similar workflow/project management tools.\n
Exposure to RFQs, change orders, contracts, and quotations.\n\n
\n
Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
","openingPlain":"Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. \n","descriptionBody":"We are seeking a full-time Bioanalytical Fee & Proposal Support professional to join our Bioanalytical Services team. In this role, you will support the development of scopes, budgets, and pricing for bioanalytical studies, working closely with Business Development, Operations, Finance, and Contracts teams.
\nThis position plays a key role in ensuring accurate, competitive, and compliant proposals while supporting the financial lifecycle of awarded studies—from forecasting through close-out.
\nProposal & Pricing Support
\n\n- Support study scoping and development of bioanalytical budgets and fee estimates.
\n- Prepare pricing materials for proposals, RFQs, bid grids, cost assumptions, and timelines.
\n- Assist with quotation and contract preparation, project number creation, and document tracking.
\n- Support change orders by evaluating scope changes and financial impacts.
\n- Maintain consistency and accuracy across pricing models, templates, and assumptions.
\n- Collaborate with cross-functional stakeholders to develop competitive pricing strategies.
\n
\nFinancial & Project Support
\n\n- Provide financial support for awarded bioanalytical projects, ensuring alignment between scope, budget, and actuals.
\n- Maintain project data in local and global systems with timely updates.
\n- Assist with weekly forecasting, variance tracking, and WIP monitoring.
\n- Support invoice preparation and allocation of pass-through costs.
\n- Partner with Finance and Contracts to ensure alignment between budgets, fees, and contractual terms.
\n- Assist with financial inquiries, adjustments, and project close-out activities.
\n
\nSystems & Process Improvement
\n\n- Support development and optimization of Smartsheet tools and pricing templates.
\n- Utilize AI and automation to improve efficiency and data accuracy.
\n- Identify opportunities for continuous improvement in proposal, pricing, and financial processes.
\n- Assist with ordering study-specific materials and supplies for the Bioanalytical department.
\n
\n
","descriptionBodyPlain":"We are seeking a full-time Bioanalytical Fee & Proposal Support professional to join our Bioanalytical Services team. In this role, you will support the development of scopes, budgets, and pricing for bioanalytical studies, working closely with Business Development, Operations, Finance, and Contracts teams.\nThis position plays a key role in ensuring accurate, competitive, and compliant proposals while supporting the financial lifecycle of awarded studies—from forecasting through close-out.\nProposal & Pricing Support\nSupport study scoping and development of bioanalytical budgets and fee estimates.\nPrepare pricing materials for proposals, RFQs, bid grids, cost assumptions, and timelines.\nAssist with quotation and contract preparation, project number creation, and document tracking.\nSupport change orders by evaluating scope changes and financial impacts.\nMaintain consistency and accuracy across pricing models, templates, and assumptions.\nCollaborate with cross-functional stakeholders to develop competitive pricing strategies.\nFinancial & Project Support\nProvide financial support for awarded bioanalytical projects, ensuring alignment between scope, budget, and actuals.\nMaintain project data in local and global systems with timely updates.\nAssist with weekly forecasting, variance tracking, and WIP monitoring.\nSupport invoice preparation and allocation of pass-through costs.\nPartner with Finance and Contracts to ensure alignment between budgets, fees, and contractual terms.\nAssist with financial inquiries, adjustments, and project close-out activities.\nSystems & Process Improvement\nSupport development and optimization of Smartsheet tools and pricing templates.\nUtilize AI and automation to improve efficiency and data accuracy.\nIdentify opportunities for continuous improvement in proposal, pricing, and financial processes.\nAssist with ordering study-specific materials and supplies for the Bioanalytical department.\n \n","hostedUrl":"https://jobs.lever.co/celerion/9d79cb5f-7597-4454-92a1-67eae3f714d3","applyUrl":"https://jobs.lever.co/celerion/9d79cb5f-7597-4454-92a1-67eae3f714d3/apply"},{"additionalPlain":"Celerion Values: Integrity Trust Teamwork Respect\n \nCelerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.\n \nNote: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as \"Not Junk\" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.\n \n","additional":"Celerion Values: Integrity Trust Teamwork Respect
\n
\nCelerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.
\n
\n\n
Note: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as \"Not Junk\" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.
\n
\n
Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
We are seeking a full-time Bioanalytical Fee & Proposal Support professional to join our Bioanalytical Services team. In this role, you will support the development of scopes, budgets, and pricing for bioanalytical studies, working closely with Business Development, Operations, Finance, and Contracts teams.
\nThis position plays a key role in ensuring accurate, competitive, and compliant proposals while supporting the financial lifecycle of awarded studies—from forecasting through close-out.
\nProposal & Pricing Support
\n\n- Support study scoping and development of bioanalytical budgets and fee estimates.
\n- Prepare pricing materials for proposals, RFQs, bid grids, cost assumptions, and timelines.
\n- Assist with quotation and contract preparation, project number creation, and document tracking.
\n- Support change orders by evaluating scope changes and financial impacts.
\n- Maintain consistency and accuracy across pricing models, templates, and assumptions.
\n- Collaborate with cross-functional stakeholders to develop competitive pricing strategies.
\n
\nFinancial & Project Support
\n\n- Provide financial support for awarded bioanalytical projects, ensuring alignment between scope, budget, and actuals.
\n- Maintain project data in local and global systems with timely updates.
\n- Assist with weekly forecasting, variance tracking, and WIP monitoring.
\n- Support invoice preparation and allocation of pass-through costs.
\n- Partner with Finance and Contracts to ensure alignment between budgets, fees, and contractual terms.
\n- Assist with financial inquiries, adjustments, and project close-out activities.
\n
\nSystems & Process Improvement
\n\n- Support development and optimization of Smartsheet tools and pricing templates.
\n- Utilize AI and automation to improve efficiency and data accuracy.
\n- Identify opportunities for continuous improvement in proposal, pricing, and financial processes.
\n- Assist with ordering study-specific materials and supplies for the Bioanalytical department.
\n
\n
","id":"b43ca37d-4a56-4110-88f9-b42aae38fad6","lists":[{"text":"Requirements","content":"\n\n
Bachelor’s degree in Business, Finance, Accounting, Life Sciences, or a related field
(or equivalent combination of education and experience).\n
2–4 years of experience in proposal support, pricing, financial operations, or project coordination.\n
Experience supporting client-facing, project-based budgets and financial tracking.\n
Strong proficiency in Microsoft Excel (advanced formulas, analysis, templates).\n
Exceptional attention to detail and commitment to data accuracy.\n
Strong analytical, organizational, and problem-solving skills.\n
Ability to manage multiple priorities in a deadline-driven environment.\n
Effective written and verbal communication skills.\n\n
\n
\n
Preferred Qualifications
\n\n
Experience in bioanalytical services, clinical research, or life sciences.\n
Familiarity with Smartsheet or similar workflow/project management tools.\n
Exposure to RFQs, change orders, contracts, and quotations.\n\n
\n
Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
","openingPlain":"Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. \n","descriptionBody":"We are seeking a full-time Bioanalytical Fee & Proposal Support professional to join our Bioanalytical Services team. In this role, you will support the development of scopes, budgets, and pricing for bioanalytical studies, working closely with Business Development, Operations, Finance, and Contracts teams.
\nThis position plays a key role in ensuring accurate, competitive, and compliant proposals while supporting the financial lifecycle of awarded studies—from forecasting through close-out.
\nProposal & Pricing Support
\n\n- Support study scoping and development of bioanalytical budgets and fee estimates.
\n- Prepare pricing materials for proposals, RFQs, bid grids, cost assumptions, and timelines.
\n- Assist with quotation and contract preparation, project number creation, and document tracking.
\n- Support change orders by evaluating scope changes and financial impacts.
\n- Maintain consistency and accuracy across pricing models, templates, and assumptions.
\n- Collaborate with cross-functional stakeholders to develop competitive pricing strategies.
\n
\nFinancial & Project Support
\n\n- Provide financial support for awarded bioanalytical projects, ensuring alignment between scope, budget, and actuals.
\n- Maintain project data in local and global systems with timely updates.
\n- Assist with weekly forecasting, variance tracking, and WIP monitoring.
\n- Support invoice preparation and allocation of pass-through costs.
\n- Partner with Finance and Contracts to ensure alignment between budgets, fees, and contractual terms.
\n- Assist with financial inquiries, adjustments, and project close-out activities.
\n
\nSystems & Process Improvement
\n\n- Support development and optimization of Smartsheet tools and pricing templates.
\n- Utilize AI and automation to improve efficiency and data accuracy.
\n- Identify opportunities for continuous improvement in proposal, pricing, and financial processes.
\n- Assist with ordering study-specific materials and supplies for the Bioanalytical department.
\n
\n
","descriptionBodyPlain":"We are seeking a full-time Bioanalytical Fee & Proposal Support professional to join our Bioanalytical Services team. In this role, you will support the development of scopes, budgets, and pricing for bioanalytical studies, working closely with Business Development, Operations, Finance, and Contracts teams.\nThis position plays a key role in ensuring accurate, competitive, and compliant proposals while supporting the financial lifecycle of awarded studies—from forecasting through close-out.\nProposal & Pricing Support\nSupport study scoping and development of bioanalytical budgets and fee estimates.\nPrepare pricing materials for proposals, RFQs, bid grids, cost assumptions, and timelines.\nAssist with quotation and contract preparation, project number creation, and document tracking.\nSupport change orders by evaluating scope changes and financial impacts.\nMaintain consistency and accuracy across pricing models, templates, and assumptions.\nCollaborate with cross-functional stakeholders to develop competitive pricing strategies.\nFinancial & Project Support\nProvide financial support for awarded bioanalytical projects, ensuring alignment between scope, budget, and actuals.\nMaintain project data in local and global systems with timely updates.\nAssist with weekly forecasting, variance tracking, and WIP monitoring.\nSupport invoice preparation and allocation of pass-through costs.\nPartner with Finance and Contracts to ensure alignment between budgets, fees, and contractual terms.\nAssist with financial inquiries, adjustments, and project close-out activities.\nSystems & Process Improvement\nSupport development and optimization of Smartsheet tools and pricing templates.\nUtilize AI and automation to improve efficiency and data accuracy.\nIdentify opportunities for continuous improvement in proposal, pricing, and financial processes.\nAssist with ordering study-specific materials and supplies for the Bioanalytical department.\n \n","hostedUrl":"https://jobs.lever.co/celerion/b43ca37d-4a56-4110-88f9-b42aae38fad6","applyUrl":"https://jobs.lever.co/celerion/b43ca37d-4a56-4110-88f9-b42aae38fad6/apply"},{"additional":"","additionalPlain":"","categories":{"commitment":"Full-Time","department":"4112 - Bioanalytical Services","location":"Fehraltorf (Zurich), Switzerland","team":"4112 - Bioanalytical Services","allLocations":["Fehraltorf (Zurich), Switzerland"]},"createdAt":1783089060066,"descriptionPlain":"Help bring tomorrow's medicines to patients.\n At Celerion Switzerland AG, part of the global Celerion Inc., we support pharmaceutical and biotechnology companies in developing innovative medicines. Our GLP-certified bioanalytical laboratory in Fehraltorf plays a key role in preclinical and clinical drug development by delivering high-quality bioanalytical data that advances life-changing therapies.\n \nAs our laboratory continues to grow, we are looking for motivated Bioanalytical Laboratory Technician to join our collaborative team. \nYour impact\nAs part of our Bioanalytical Laboratory, you will contribute directly to drug development by performing high-quality analyses in a regulated laboratory environment.\n","description":"\n
Help bring tomorrow's medicines to patients.
\nAt
Celerion Switzerland AG, part of the global
Celerion Inc., we support pharmaceutical and biotechnology companies in developing innovative medicines. Our GLP-certified bioanalytical laboratory in Fehraltorf plays a key role in preclinical and clinical drug development by delivering high-quality bioanalytical data that advances life-changing therapies.
\nAs our laboratory continues to grow, we are looking for motivated
Bioanalytical Laboratory Technician to join our collaborative team.\n
Your impact
\n
As part of our Bioanalytical Laboratory, you will contribute directly to drug development by performing high-quality analyses in a regulated laboratory environment.
\n
Depending on your experience and area of expertise, your responsibilities include:
\n\nPerforming bioanalytical measurements of pharmaceutical compounds in biological samples using immunoassay-based (LBS) or LC-MS/MS methods\nPreparing biological samples and operating modern LC-MS/MS instrumentation (LC-MS position)\nPlanning, executing and documenting bioanalytical assays in accordance with GLP requirements\nPerforming method validations and supporting preclinical and clinical study analyses\nEvaluating analytical results and ensuring data quality and integrity\nParticipating in routine laboratory organization, equipment maintenance and quality activities\nContributing to continuous improvement of laboratory processes\n"},{"text":"Your Profile","content":"\nCompleted vocational training as a Chemical, Biological or Medical Laboratory Technician (CTA, BTA, MTA or equivalent)\nExperience working with biological samples\nStrong knowledge of biochemistry, analytical chemistry and/or chromatography and mass spectrometry\nCareful, structured and quality-focused working style\nGood documentation skills and attention to detail\nGood communication skills in both German and English\nExperience working in a regulated environment (GLP, GCP, GMP or ISO) is an advantage\n"},{"text":"Why join Celerion?","content":"At Celerion, you'll become part of an international organization where your work has a direct impact on the development of new medicines. We value teamwork, scientific excellence and continuous learning.
\nWe offer:
\n\nA meaningful role supporting innovative drug development\nA collaborative, supportive and experienced laboratory team\nComprehensive onboarding and structured training\nOpportunities for professional growth and development\nModern, state-of-the-art laboratory facilities\nDiverse and technically challenging projects\nFlexible working hours that support work-life balance\nAttractive employment conditions within a stable and growing international company\n\nInterested?
\nWe would love to hear from you.
"}],"text":"Bioanalytical Laboratory Technician (80 - 100%)","country":"CH","workplaceType":"onsite","opening":"","openingPlain":"","descriptionBody":"\n
Help bring tomorrow's medicines to patients.
\nAt
Celerion Switzerland AG, part of the global
Celerion Inc., we support pharmaceutical and biotechnology companies in developing innovative medicines. Our GLP-certified bioanalytical laboratory in Fehraltorf plays a key role in preclinical and clinical drug development by delivering high-quality bioanalytical data that advances life-changing therapies.
\nAs our laboratory continues to grow, we are looking for motivated
Bioanalytical Laboratory Technician to join our collaborative team.\n
Your impact
\n
As part of our Bioanalytical Laboratory, you will contribute directly to drug development by performing high-quality analyses in a regulated laboratory environment.
\n
Celerion Values: Integrity Trust Teamwork Respect
\n
\nCelerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.
\n
\n\n
Note: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as \"Not Junk\" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.
\n
\n
Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
Are you looking for an opportunity to support a business creating life-saving treatments? If so, we can't wait to meet you!
\n
\nLocation: Corporate office in Lincoln, NE. Just south of downtown.
\n
\nAs a Bioanalytical Principal Investigator, you will have overall responsibility for the technical conduct of the bioanalytical portion of studies. This role is with our Small Molecule team.
\n
","id":"a8b1690d-a337-45ce-abc7-7d53555139ff","lists":[{"text":"Essential Functions:","content":"\nServe as primary client contact for the bioanalytical segment of studies\nReview protocol and assure study is conducted in accordance with Protocol\nDocument and report any deviations from the protocol to Study Director or Sponsor\nReview and approve Sample Analysis Plans\nAssure all experimental data is accurately recorded and verified\nAssure corrective action is taken and documented when necessary\nReview and approve all project-related QA audits\nApprove and document any bioanalytical deviations\nReview and approve all bioanalytical reports\nAssure all study personnel have adequate training, education and experience to perform required study functions\nConduct impact analysis of bioanalytical deviations\nOversight of Event Investigation reports\n"},{"text":"Requirements:","content":"\nMinimum of a Bachelor's degree or equivalent in a science-related field with 5 or more years of industry experience preferred\n5 or more years of previous laboratory and/or regulated bioanalysis knowledge preferred\nProficiency with computers \nExcellent oral and written skills \n"}],"text":"Bioanalytical Principal Investigator - Small Molecule","country":"US","workplaceType":"onsite","opening":"Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
","openingPlain":"Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. \n","descriptionBody":"Are you looking for an opportunity to support a business creating life-saving treatments? If so, we can't wait to meet you!
\n
\nLocation: Corporate office in Lincoln, NE. Just south of downtown.
\n
\nAs a Bioanalytical Principal Investigator, you will have overall responsibility for the technical conduct of the bioanalytical portion of studies. This role is with our Small Molecule team.
\n
","descriptionBodyPlain":"Are you looking for an opportunity to support a business creating life-saving treatments? If so, we can't wait to meet you!\n \nLocation: Corporate office in Lincoln, NE. Just south of downtown.\n \nAs a Bioanalytical Principal Investigator, you will have overall responsibility for the technical conduct of the bioanalytical portion of studies. This role is with our Small Molecule team.\n \n","hostedUrl":"https://jobs.lever.co/celerion/a8b1690d-a337-45ce-abc7-7d53555139ff","applyUrl":"https://jobs.lever.co/celerion/a8b1690d-a337-45ce-abc7-7d53555139ff/apply"},{"additionalPlain":"If you are a Gmail user and you chose to receive e-mails from @celerion.com, please check your Spam folder regarding the status of your application, including requests for availability and interview invitations. Additionally, ensure you mark Celerion e-mails as “Not Junk”.\n\n\nCelerion Values: Integrity Trust Teamwork Respect\n \nCelerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.\n \nNote: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as \"Not Junk\" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.\n \n","additional":"If you are a Gmail user and you chose to receive e-mails from @celerion.com, please check your Spam folder regarding the status of your application, including requests for availability and interview invitations. Additionally, ensure you mark Celerion e-mails as “Not Junk”.
Celerion Values: Integrity Trust Teamwork Respect
\n
\nCelerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.
\n
\n\n
Note: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as \"Not Junk\" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.
\n
\n
Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
We are seeking a Clinical Research Coordinator to join our Lincoln, NE team! This is a great opportunity for someone seeking a career change. Training is provided.
\nAs a Clinical Research Coordinator you are responsible for oversight and conduct of clinical studies. You will ensure compliance, quality, and profitability of clinical studies. You respond to internal and external client issues, concerns, and requests by applying study management techniques and tools. In this role you should plan to work some evening and weekends.
\n
\nPrimary Responsibilities:
\nYou are responsible for the overall management of Clinical Studies to include: on-time performance with defect-free execution, independently conducting bioequivalency and bioavailability studies, working with support divisions to ensure timelines are being met in clinical studies (i.e. recruiting, data management, statistics), organizing study initiation meetings to plan execution of study, facilitating study review meetings for pre-study, in-process and post study review, problem solving as needed during study conduct, meeting with clients as needed throughout study, and organizing study logistics and personnel. In addition, you will be present at critical events and dosings of study. You will build client relationships that result in additional business, you will craft and edit reports, respond to client issues, concerns and requests, adhere to milestone guidelines, and ensure profitability by maintaining profitability of team through a budgeting and expense control on a total and individual study basis.
\n
","id":"95f073c3-2d07-4955-a6d4-6f9bebd1ba13","lists":[{"text":"Requirements","content":"\nYou will have a Bachelor’s degree in a related discipline or BSN required. Celerion experience may be considered in lieu of degree in some situations.\nIndustry experience and knowledge of medical terminology preferred.\nDemonstrated organizational, time management and multi-tasking skills required\nShown ability to handle multiple priorities\nExcellent oral and written communication skills\nYou will work without close supervision\nAbility to work flexible hours required for study conduct\nYou will utilize customer service skills\nClinical Research experience useful, but not required\n"}],"text":"Clinical Research Coordinator","country":"US","workplaceType":"onsite","opening":"Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
","openingPlain":"Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. \n","descriptionBody":"We are seeking a Clinical Research Coordinator to join our Lincoln, NE team! This is a great opportunity for someone seeking a career change. Training is provided.
\nAs a Clinical Research Coordinator you are responsible for oversight and conduct of clinical studies. You will ensure compliance, quality, and profitability of clinical studies. You respond to internal and external client issues, concerns, and requests by applying study management techniques and tools. In this role you should plan to work some evening and weekends.
\n
\nPrimary Responsibilities:
\nYou are responsible for the overall management of Clinical Studies to include: on-time performance with defect-free execution, independently conducting bioequivalency and bioavailability studies, working with support divisions to ensure timelines are being met in clinical studies (i.e. recruiting, data management, statistics), organizing study initiation meetings to plan execution of study, facilitating study review meetings for pre-study, in-process and post study review, problem solving as needed during study conduct, meeting with clients as needed throughout study, and organizing study logistics and personnel. In addition, you will be present at critical events and dosings of study. You will build client relationships that result in additional business, you will craft and edit reports, respond to client issues, concerns and requests, adhere to milestone guidelines, and ensure profitability by maintaining profitability of team through a budgeting and expense control on a total and individual study basis.
\n
","descriptionBodyPlain":"We are seeking a Clinical Research Coordinator to join our Lincoln, NE team! This is a great opportunity for someone seeking a career change. Training is provided.\nAs a Clinical Research Coordinator you are responsible for oversight and conduct of clinical studies. You will ensure compliance, quality, and profitability of clinical studies. You respond to internal and external client issues, concerns, and requests by applying study management techniques and tools. In this role you should plan to work some evening and weekends.\n \nPrimary Responsibilities:\nYou are responsible for the overall management of Clinical Studies to include: on-time performance with defect-free execution, independently conducting bioequivalency and bioavailability studies, working with support divisions to ensure timelines are being met in clinical studies (i.e. recruiting, data management, statistics), organizing study initiation meetings to plan execution of study, facilitating study review meetings for pre-study, in-process and post study review, problem solving as needed during study conduct, meeting with clients as needed throughout study, and organizing study logistics and personnel. In addition, you will be present at critical events and dosings of study. You will build client relationships that result in additional business, you will craft and edit reports, respond to client issues, concerns and requests, adhere to milestone guidelines, and ensure profitability by maintaining profitability of team through a budgeting and expense control on a total and individual study basis.\n \n","hostedUrl":"https://jobs.lever.co/celerion/95f073c3-2d07-4955-a6d4-6f9bebd1ba13","applyUrl":"https://jobs.lever.co/celerion/95f073c3-2d07-4955-a6d4-6f9bebd1ba13/apply"},{"additionalPlain":"Shift\nAvailability for 4 x 10hrs shifts from 0500-1700\nAbility to work one weekend per month\n \n \nIf you are a Gmail user and you chose to receive e-mails from @celerion.com, please check your Spam folder regarding the status of your application, including requests for availability and interview invitations. Additionally, ensure you mark Celerion e-mails as “Not Junk”.\n\n\nCelerion Values: Integrity Trust Teamwork Respect\n \nCelerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.\n \nNote: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as \"Not Junk\" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.\n \n","additional":"\n
Shift
\n
Availability for 4 x 10hrs shifts from 0500-1700
\n
Ability to work one weekend per month
\n
\n
\n
If you are a Gmail user and you chose to receive e-mails from @celerion.com, please check your Spam folder regarding the status of your application, including requests for availability and interview invitations. Additionally, ensure you mark Celerion e-mails as “Not Junk”.
\n
Celerion Values: Integrity Trust Teamwork Respect
\n
\nCelerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.
\n
\n\n
Note: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as \"Not Junk\" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.
\n
\n
Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
Celerion is seeking a Full-time day shift Research Nurse to assist with our clinical research trials. This is a dynamic role working with a healthy population offering the ability to learn about clinical research and see the drug development process at work.
\n
\nAre you looking for an opportunity that will make a difference in the future of health care? If so, we can't wait to meet you. Do you want to learn more?
","id":"40d0a7a0-ead8-408e-9f98-529e820d8743","lists":[{"text":"Responsibilities","content":"\nYou will be responsible for performing scheduled events according to the study protocol.\nYou will work directly with study managers to successfully ensure a successful trial.\nYou will work with participants in the research process, under our care, doing vital sign checks, ECGs, blood draws and telemetry monitoring.\nYou will also identify and report adverse events to assist in the clinical research process.\n"},{"text":"Qualifications","content":"\nYou will have a current NE RN or LPN license and clinical assessment skills\nYour ACLS certification is a plus\nStrong computer and documentation skills\n"}],"text":"Clinical Research Nurse (FT Days)","country":"US","workplaceType":"onsite","opening":"Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
","openingPlain":"Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. \n","descriptionBody":"Celerion is seeking a Full-time day shift Research Nurse to assist with our clinical research trials. This is a dynamic role working with a healthy population offering the ability to learn about clinical research and see the drug development process at work.
\n
\nAre you looking for an opportunity that will make a difference in the future of health care? If so, we can't wait to meet you. Do you want to learn more?
","descriptionBodyPlain":"Celerion is seeking a Full-time day shift Research Nurse to assist with our clinical research trials. This is a dynamic role working with a healthy population offering the ability to learn about clinical research and see the drug development process at work.\n \nAre you looking for an opportunity that will make a difference in the future of health care? If so, we can't wait to meet you. Do you want to learn more?\n","hostedUrl":"https://jobs.lever.co/celerion/40d0a7a0-ead8-408e-9f98-529e820d8743","applyUrl":"https://jobs.lever.co/celerion/40d0a7a0-ead8-408e-9f98-529e820d8743/apply"},{"additionalPlain":"Shift:\nYou should be available to work the following scheduling availability:\n* Mon- Sun from 1300-2330 (clock in will be from 1300-1500)\n* One weekend (Saturday and Sunday) a month. \n* Shifts can be 5x8 or 4 x10 based on employee preference\n \n \n\n\nCelerion Values: Integrity Trust Teamwork Respect\n \nCelerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.\n \nNote: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as \"Not Junk\" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.\n \n","additional":"Shift:
\nYou should be available to work the following scheduling availability:
\n* Mon- Sun from 1300-2330 (clock in will be from 1300-1500)
\n* One weekend (Saturday and Sunday) a month.
\n* Shifts can be 5x8 or 4 x10 based on employee preference
\n
\n
Celerion Values: Integrity Trust Teamwork Respect
\n
\nCelerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.
\n
\n\n
Note: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as \"Not Junk\" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.
\n
\n
Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
Celerion is seeking a Full-time evening shift Research Nurse to assist with our clinical research trials. This is a dynamic role working with a healthy population offering the ability to learn about clinical research and see the drug development process at work.
\n
\nAre you looking for an opportunity that will make a difference in the future of health care? If so, we can't wait to meet you. Do you want to learn more?
","id":"1ebdc03e-d01e-4392-afe3-a5ea2170b50e","lists":[{"text":"Responsibilities","content":"\nYou will be responsible for performing scheduled events according to the study protocol.\nYou will work directly with study managers to successfully ensure a successful trial.\nYou will work with participants in the research process, under our care, doing vital sign checks, ECGs, blood draws and telemetry monitoring.\nYou will also identify and report adverse events to assist in the clinical research process.\n"},{"text":"Qualifications","content":"\nYou will have a current NE RN or LPN license and clinical assessment skills\nYour ACLS certification is a plus\nStrong computer and documentation skills\n"}],"text":"Clinical Research Nurse (FT Evenings)","country":"US","workplaceType":"onsite","opening":"Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
","openingPlain":"Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. \n","descriptionBody":"Celerion is seeking a Full-time evening shift Research Nurse to assist with our clinical research trials. This is a dynamic role working with a healthy population offering the ability to learn about clinical research and see the drug development process at work.
\n
\nAre you looking for an opportunity that will make a difference in the future of health care? If so, we can't wait to meet you. Do you want to learn more?
","descriptionBodyPlain":"Celerion is seeking a Full-time evening shift Research Nurse to assist with our clinical research trials. This is a dynamic role working with a healthy population offering the ability to learn about clinical research and see the drug development process at work.\n \nAre you looking for an opportunity that will make a difference in the future of health care? If so, we can't wait to meet you. Do you want to learn more?\n","hostedUrl":"https://jobs.lever.co/celerion/1ebdc03e-d01e-4392-afe3-a5ea2170b50e","applyUrl":"https://jobs.lever.co/celerion/1ebdc03e-d01e-4392-afe3-a5ea2170b50e/apply"},{"additionalPlain":"Celerion Values: Integrity Trust Teamwork Respect\n \nCelerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.\n \nNote: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as \"Not Junk\" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.\n \n","additional":"Celerion Values: Integrity Trust Teamwork Respect
\n
\nCelerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.
\n
\n\n
Note: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as \"Not Junk\" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.
\n
\n
Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
We are currently seeking a full time Clinical Study Designer at our Lincoln, Nebraska location. As part of our team, you will be responsible for the logistical set up and maintenance of clinical trials in ClinQuick - our electronic data capture system. You will also manage the creation of study conduct instruction manuals and detailed timed event schedules for the clinic staff and study participants.
\n
\nRequirements:
\nA minimum of an Associate’s degree in a health related field and/or applicable experience in a medical, clinical, pharmaceutical or laboratory setting is required. You must be detail‑oriented, computer literate, and able to work in a fast-paced atmosphere.
","id":"36431cdb-3b2a-4488-ac33-e5ac3b46b51e","lists":[],"salaryRange":{"min":20,"max":21,"currency":"USD","interval":"per-hour-wage"},"text":"Clinical Study Designer - Lincoln, Nebraska","country":"US","workplaceType":"hybrid","opening":"Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
","openingPlain":"Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. \n","descriptionBody":"We are currently seeking a full time Clinical Study Designer at our Lincoln, Nebraska location. As part of our team, you will be responsible for the logistical set up and maintenance of clinical trials in ClinQuick - our electronic data capture system. You will also manage the creation of study conduct instruction manuals and detailed timed event schedules for the clinic staff and study participants.
\n
\nRequirements:
\nA minimum of an Associate’s degree in a health related field and/or applicable experience in a medical, clinical, pharmaceutical or laboratory setting is required. You must be detail‑oriented, computer literate, and able to work in a fast-paced atmosphere.
","descriptionBodyPlain":"We are currently seeking a full time Clinical Study Designer at our Lincoln, Nebraska location. As part of our team, you will be responsible for the logistical set up and maintenance of clinical trials in ClinQuick - our electronic data capture system. You will also manage the creation of study conduct instruction manuals and detailed timed event schedules for the clinic staff and study participants. \n \nRequirements:\nA minimum of an Associate’s degree in a health related field and/or applicable experience in a medical, clinical, pharmaceutical or laboratory setting is required. You must be detail‑oriented, computer literate, and able to work in a fast-paced atmosphere.\n","hostedUrl":"https://jobs.lever.co/celerion/36431cdb-3b2a-4488-ac33-e5ac3b46b51e","applyUrl":"https://jobs.lever.co/celerion/36431cdb-3b2a-4488-ac33-e5ac3b46b51e/apply"},{"additionalPlain":"Celerion are an equal opportunities employer\n","additional":"Celerion are an equal opportunities employer
","categories":{"commitment":"Full-Time","department":"Job Posting Categories","location":"Belfast, Northern Ireland","team":"Clinical Data Sciences","allLocations":["Belfast, Northern Ireland"]},"createdAt":1786004869537,"descriptionPlain":"Join a team that's going places!\nEvery member of Celerion is involved in making a distinctive contribution to the health and well-being of people around the world. That's the sense of purpose shared by our employees. We are a performance-driven drug research company, operating in robust and growing markets. We have an exciting future and offer a strong development environment for our great employees.\nCome be part of our Data Management and Biometrics team as a Data Programmer.\nThis full-time position will be attached to our Belfast, Northern Ireland clinical trial facility with a work-from-home/hybrid working arrangement available within the UK. \nThe purpose of the Data Programmer role is to develop and support clinical database programming activities and associated documentation involved in clinical trial set-up, conduct and close-out stages in line with protocol requirements, standard operating procedures (SOPs/PGs), Good Clinical Programming Practices (GXP), Clinical Data Interchange Standards (CDISC) and other applicable sponsor or regulatory requirements.\nEssential Functions:\nSAS Pre-lock programming - Deliver and support all pre-database lock SAS programming processes associated with data collection, reporting and cleaning\nData import and integration - Support data import programming and reconciliation activities as needed\nData transfer programming - Deliver and support raw/CDASH, lab only, CDISC/SDTM or sponsor specified custom data transfers\nProcess Improvements - Actively participate in process improvement initiatives\nQuality/timelines - Ensure that data programming delivers quality outputs on time or better following good programming practices, including adequately-documented SAS code\nThis full-time position has an attractive salary and benefits package including pension, life assurance, permanent health insurance and private medical insurance. \nTraining will be provided on clinical research data programming skills.\n","description":"\n
Join a team that's going places!
\n
\n
Every member of Celerion is involved in making a distinctive contribution to the health and well-being of people around the world. That's the sense of purpose shared by our employees. We are a performance-driven drug research company, operating in robust and growing markets. We have an exciting future and offer a strong development environment for our great employees.
\n
\n
Come be part of our Data Management and Biometrics team as a Data Programmer.
\n
\n
This full-time position will be attached to our Belfast, Northern Ireland clinical trial facility with a work-from-home/hybrid working arrangement available within the UK.
\n
\n
The purpose of the Data Programmer role is to develop and support clinical database programming activities and associated documentation involved in clinical trial set-up, conduct and close-out stages in line with protocol requirements, standard operating procedures (SOPs/PGs), Good Clinical Programming Practices (GXP), Clinical Data Interchange Standards (CDISC) and other applicable sponsor or regulatory requirements.
\n
\n- SAS Pre-lock programming - Deliver and support all pre-database lock SAS programming processes associated with data collection, reporting and cleaning
\n- Data import and integration - Support data import programming and reconciliation activities as needed
\n- Data transfer programming - Deliver and support raw/CDASH, lab only, CDISC/SDTM or sponsor specified custom data transfers
\n- Process Improvements - Actively participate in process improvement initiatives
\n- Quality/timelines - Ensure that data programming delivers quality outputs on time or better following good programming practices, including adequately-documented SAS code
\n
\n\n
This full-time position has an attractive salary and benefits package including pension, life assurance, permanent health insurance and private medical insurance.
\n
\n
Training will be provided on clinical research data programming skills.
\n
\n
\n- Bachelor's degree with 1+ yrs programming experience OR comparable experience in related industry, previous experience with SAS and clinical data preferred.
\n- Computer science, Mathematics or IT graduate applicants also considered.
\n- Demonstrated communication and interpersonal skills
\n- Demonstrated problem solving and decision making skills
\n- Demonstrated ability to manage multiple priorities
\n- Internal Celerion candidates with strong clinical data review, data management or IT background will also be considered.
\n\n
\n
Join a team that's going places!
\n
\n
Every member of Celerion is involved in making a distinctive contribution to the health and well-being of people around the world. That's the sense of purpose shared by our employees. We are a performance-driven drug research company, operating in robust and growing markets. We have an exciting future and offer a strong development environment for our great employees.
\n
\n
Come be part of our Data Management and Biometrics team as a Data Programmer.
\n
\n
This full-time position will be attached to our Belfast, Northern Ireland clinical trial facility with a work-from-home/hybrid working arrangement available within the UK.
\n
\n
The purpose of the Data Programmer role is to develop and support clinical database programming activities and associated documentation involved in clinical trial set-up, conduct and close-out stages in line with protocol requirements, standard operating procedures (SOPs/PGs), Good Clinical Programming Practices (GXP), Clinical Data Interchange Standards (CDISC) and other applicable sponsor or regulatory requirements.
\n
\n- SAS Pre-lock programming - Deliver and support all pre-database lock SAS programming processes associated with data collection, reporting and cleaning
\n- Data import and integration - Support data import programming and reconciliation activities as needed
\n- Data transfer programming - Deliver and support raw/CDASH, lab only, CDISC/SDTM or sponsor specified custom data transfers
\n- Process Improvements - Actively participate in process improvement initiatives
\n- Quality/timelines - Ensure that data programming delivers quality outputs on time or better following good programming practices, including adequately-documented SAS code
\n
\n\n
This full-time position has an attractive salary and benefits package including pension, life assurance, permanent health insurance and private medical insurance.
\n
\n
Training will be provided on clinical research data programming skills.
\n
Celerion Values: Integrity Trust Teamwork Respect
\n
\nCelerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.
\n
\n\n
Note: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as \"Not Junk\" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.
\n
\n
Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
Are you looking for an opportunity to support a business creating life-saving treatments? If so, we can't wait to meet you!
\n
\nWe are looking for a performance-oriented, innovative and self-motivated team player to join our Clinical Data Sciences team as a full-time Electronic Data Capture (EDC) Database Developer / Clinical Programmer. You will be responsible for administration of EDC Database including evaluation, analysis, design and/ or recommendations to achieve goals and excellent results in a fast-paced, ever-changing environment.
\n
\nThis is a full time, remote opportunity, but may travel for training and key meetings.
\n
\nAs an EDC Database Developer, you will build and administer EDC trials for client contracted projects including protocol/requirements evaluation, electronic case report form (eCRF) design and build with corresponding edits. This role will have technical interaction with vendors that are supporting the applications and troubleshoot/ escalate problems on systems to appropriate partners. This role will provide expert guidance to the design, development, validation, implementation and maintenance of study set-up. Additionally, this role will manage the deployment of EDC trials and set up interface connections between EDC and other systems.
\n
","id":"a809b686-be73-4f33-b234-c6079032eda1","lists":[{"text":"In this role you will:","content":"\nServe as a subject matter expert in Veeva Clinical Data Management Suite (CDMS), including Veeva Electronic Data Capture (EDC) and Veeva Clinical Database (CDB)\nPerform all activities related to eCRF design and EDC build programming for assigned projects\nPerform EDC edit check programming for assigned projects based on edit check specifications for both simple and complex edit checks\nCreate test data to verify both screen design and edit check programming prior to deploying to User Acceptance Testing (UAT)\nSet up test environments and coordinate project team members for execution of test scripts\nProgram and configure listings and reports using clinical reporting tools such as Veeva Clinical Database (CDB)\nEnsure secure and high-integrity database imports from vendor transfers using Celerion data transfer standards\nAssist with the validation of upgrades to hardware/ software including validation documentation development, review and execution.\nMaintain global clinical trial database standards (CDISC)\n"},{"text":"Requirements:","content":"\nBachelor’s degree in a related field preferred\n3 years of clinical data management experience\nAbility to program using SQL required\nExperience with EDC systems (i.e. Veeva CDMS, Medidata RAVE, etc.)\nExperience with Veeva EDC and Veeva CDB preferred\nProficient computer skills with understanding of clinical systems and data administration\nMust be organized, an effective written and oral communicator\nMust have the ability to multi-task, within a fast-paced environment, and build strong relationships \n\n
\n#LI-Remote
"}],"text":"EDC Developer / Programmer","country":"US","workplaceType":"remote","opening":"Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
","openingPlain":"Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. \n","descriptionBody":"Are you looking for an opportunity to support a business creating life-saving treatments? If so, we can't wait to meet you!
\n
\nWe are looking for a performance-oriented, innovative and self-motivated team player to join our Clinical Data Sciences team as a full-time Electronic Data Capture (EDC) Database Developer / Clinical Programmer. You will be responsible for administration of EDC Database including evaluation, analysis, design and/ or recommendations to achieve goals and excellent results in a fast-paced, ever-changing environment.
\n
\nThis is a full time, remote opportunity, but may travel for training and key meetings.
\n
\nAs an EDC Database Developer, you will build and administer EDC trials for client contracted projects including protocol/requirements evaluation, electronic case report form (eCRF) design and build with corresponding edits. This role will have technical interaction with vendors that are supporting the applications and troubleshoot/ escalate problems on systems to appropriate partners. This role will provide expert guidance to the design, development, validation, implementation and maintenance of study set-up. Additionally, this role will manage the deployment of EDC trials and set up interface connections between EDC and other systems.
\n
","descriptionBodyPlain":"Are you looking for an opportunity to support a business creating life-saving treatments? If so, we can't wait to meet you!\n \nWe are looking for a performance-oriented, innovative and self-motivated team player to join our Clinical Data Sciences team as a full-time Electronic Data Capture (EDC) Database Developer / Clinical Programmer. You will be responsible for administration of EDC Database including evaluation, analysis, design and/ or recommendations to achieve goals and excellent results in a fast-paced, ever-changing environment.\n \nThis is a full time, remote opportunity, but may travel for training and key meetings.\n \nAs an EDC Database Developer, you will build and administer EDC trials for client contracted projects including protocol/requirements evaluation, electronic case report form (eCRF) design and build with corresponding edits. This role will have technical interaction with vendors that are supporting the applications and troubleshoot/ escalate problems on systems to appropriate partners. This role will provide expert guidance to the design, development, validation, implementation and maintenance of study set-up. Additionally, this role will manage the deployment of EDC trials and set up interface connections between EDC and other systems.\n \n","hostedUrl":"https://jobs.lever.co/celerion/a809b686-be73-4f33-b234-c6079032eda1","applyUrl":"https://jobs.lever.co/celerion/a809b686-be73-4f33-b234-c6079032eda1/apply"},{"additionalPlain":"Celerion Values: Integrity Trust Teamwork Respect\n \nCelerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.\n \nNote: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as \"Not Junk\" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.\n \n","additional":"Celerion Values: Integrity Trust Teamwork Respect
\n
\nCelerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.
\n
\n\n
Note: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as \"Not Junk\" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.
\n
\n
Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
Celerion has a 2nd shift full-time position open as a Laboratory Instrument Technician – HPLC/LCMS in our Bioanalytical Division in Lincoln, NE.
\n
\nDo you have an interest in, or basic knowledge of, HPLC or LC/MS/MS techniques? If so, this could be the position for you! In this role, you will be responsible for performing analytical analysis of samples using chromatography and mass spectrometry in our nicotine-free laboratory environment.
\n
\nWe are only considering candidates currently local to Lincoln, NE at this time. This role starts at $22 per hour, plus a 5% shift differential.
\nResponsibilities:
\n\n
\n- The hired candidate will be trained to set up, operate, evaluate, monitor, troubleshoot system issues, instrument batches, and perform routine maintenance to the level of training on HPLC, and LC-MS/MS systems
\n- Responsible for completing the minimum assigned daily lab duties of 4 batches
\n- Take inventory of systems and equipment, active in column organization, prepare mobile phase and solutions
\n- Document clearly and accurately, and create, edit, and troubleshoot run sheets
\n- Proficient with all required quantification software programs
\n
\n
Requirements:
\n
\n
\n- Experience in Mass spectrometry is preferred but is not required
\n- Previous coursework in chemistry or a related field, with a degree preferred
\n- Strong mechanical inclination is a plus
\n- We are seeking candidates with working knowledge of GLP’s.
\n- Basic knowledge of computers is also required
\n- Bona Fide Occupational Qualification: This position requires candidates to be a non-nicotine/ tobacco user. This role is responsible for preparing solutions that cannot be contaminated with nicotine. This position is in continuous contact with the main glassware storage area which cannot be contaminated with nicotine. Nicotine is a volatile compound and a nicotine user simply being in the same room as the glassware can raise the nicotine levels in that glassware above our limit of detection and cause contamination issues in regards to our studies
\n
\n
\n
Shift:
\n
\n- Monday-Friday 4PM - 12:30AM, this position offers base plus shift differential
\n- Occasional weekend availability as needed
\n
\n
\n
Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
","openingPlain":"Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. \n","descriptionBody":"Celerion has a 2nd shift full-time position open as a Laboratory Instrument Technician – HPLC/LCMS in our Bioanalytical Division in Lincoln, NE.
\n
\nDo you have an interest in, or basic knowledge of, HPLC or LC/MS/MS techniques? If so, this could be the position for you! In this role, you will be responsible for performing analytical analysis of samples using chromatography and mass spectrometry in our nicotine-free laboratory environment.
\n
\nWe are only considering candidates currently local to Lincoln, NE at this time. This role starts at $22 per hour, plus a 5% shift differential.
\nResponsibilities:
\n\n
\n- The hired candidate will be trained to set up, operate, evaluate, monitor, troubleshoot system issues, instrument batches, and perform routine maintenance to the level of training on HPLC, and LC-MS/MS systems
\n- Responsible for completing the minimum assigned daily lab duties of 4 batches
\n- Take inventory of systems and equipment, active in column organization, prepare mobile phase and solutions
\n- Document clearly and accurately, and create, edit, and troubleshoot run sheets
\n- Proficient with all required quantification software programs
\n
\n
Requirements:
\n
\n
\n- Experience in Mass spectrometry is preferred but is not required
\n- Previous coursework in chemistry or a related field, with a degree preferred
\n- Strong mechanical inclination is a plus
\n- We are seeking candidates with working knowledge of GLP’s.
\n- Basic knowledge of computers is also required
\n- Bona Fide Occupational Qualification: This position requires candidates to be a non-nicotine/ tobacco user. This role is responsible for preparing solutions that cannot be contaminated with nicotine. This position is in continuous contact with the main glassware storage area which cannot be contaminated with nicotine. Nicotine is a volatile compound and a nicotine user simply being in the same room as the glassware can raise the nicotine levels in that glassware above our limit of detection and cause contamination issues in regards to our studies
\n
\n
\n
Shift:
\n
\n- Monday-Friday 4PM - 12:30AM, this position offers base plus shift differential
\n- Occasional weekend availability as needed
\n
\n
\n
Celerion Values: Integrity Trust Teamwork Respect
\n
\nCelerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.
\n
\n\n
Note: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as \"Not Junk\" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.
\n
\n
Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
We're seeking an Instrument Scientist to join our Dose Formulation team at our facility in Lincoln, NE, located just south of downtown.
\n
\nIn this lab-based role, you'll execute critical tests to ensure compounds from our in-house pharmacy meet all required specifications for use in clinical research trials.
\n
\nIf you're driven by tight timelines and passionate about advancing human health, this could be the role for you. You'll leverage your expertise in analytical chemistry to ensure every dose is ready for delivery on schedule.
\n
\nEssential Functions:
\n\n
\n- Partner with senior scientists to develop chromatographic in support of dose formulation testing
\n- Complete tasks necessary for daily operation in the laboratory: execute analytical tests to ensure the accuracy, homogeneity and precision to support on-site compounding by the Celerion Pharmacy team.
\n- Preparation of standard calibrators, quality controls, mobile phases, and solutions for the purpose of testing dose formulations.
\n- Inventory and re-order parts when used for instrument maintenance and repair
\n- Assist in troubleshooting instrumentation aspects of studies
\n- Take part in instrumentation upkeep by observing the maintenance schedule and performing calibrations and preventative maintenance
\n- Communicate results effectively and in a timely manner to other associates
\n- Initiate, introduce, and implement new guidelines and procedures through the development of working instructions
\n- Optimize instruments to support ruggedness testing, production flexibility, and production
\n- Prepare documentation to share method development results with the sponsor
\n- Write detailed methodologies and provide feedback on Dose Formulation Protocols.
\n
\n
Requirements:
\n
\n
\n
\n- Bachelor's degree in Chemistry, Biochemistry, or related scientific field, advanced degree is a plus
\n- 3-5 years of post-academic hands-on experience with analytical instrumentation and/or method development (highly preferred)
\n- Self-directed, self-motivated, and detail-oriented
\n- Strong desire to learn new techniques with openness to cross-training opportunities
\n- Flexibility to work outside normal business hours as needed to meet testing timelines, including occasional long days, evenings and weekends
\n
\n
\n
Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
","openingPlain":"Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. \n","descriptionBody":"We're seeking an Instrument Scientist to join our Dose Formulation team at our facility in Lincoln, NE, located just south of downtown.
\n
\nIn this lab-based role, you'll execute critical tests to ensure compounds from our in-house pharmacy meet all required specifications for use in clinical research trials.
\n
\nIf you're driven by tight timelines and passionate about advancing human health, this could be the role for you. You'll leverage your expertise in analytical chemistry to ensure every dose is ready for delivery on schedule.
\n
\nEssential Functions:
\n\n
\n- Partner with senior scientists to develop chromatographic in support of dose formulation testing
\n- Complete tasks necessary for daily operation in the laboratory: execute analytical tests to ensure the accuracy, homogeneity and precision to support on-site compounding by the Celerion Pharmacy team.
\n- Preparation of standard calibrators, quality controls, mobile phases, and solutions for the purpose of testing dose formulations.
\n- Inventory and re-order parts when used for instrument maintenance and repair
\n- Assist in troubleshooting instrumentation aspects of studies
\n- Take part in instrumentation upkeep by observing the maintenance schedule and performing calibrations and preventative maintenance
\n- Communicate results effectively and in a timely manner to other associates
\n- Initiate, introduce, and implement new guidelines and procedures through the development of working instructions
\n- Optimize instruments to support ruggedness testing, production flexibility, and production
\n- Prepare documentation to share method development results with the sponsor
\n- Write detailed methodologies and provide feedback on Dose Formulation Protocols.
\n
\n
Requirements:
\n
\n
\n
\n- Bachelor's degree in Chemistry, Biochemistry, or related scientific field, advanced degree is a plus
\n- 3-5 years of post-academic hands-on experience with analytical instrumentation and/or method development (highly preferred)
\n- Self-directed, self-motivated, and detail-oriented
\n- Strong desire to learn new techniques with openness to cross-training opportunities
\n- Flexibility to work outside normal business hours as needed to meet testing timelines, including occasional long days, evenings and weekends
\n
\n
\n
Celerion Values: Integrity Trust Teamwork Respect
\n
\nCelerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.
\n
\n\n
Note: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as \"Not Junk\" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.
\n
\n
Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
Do you have basic knowledge of Chromatography or Ligand-Binding techniques and laboratory experience? If so, this could be the position for you! This is a great opportunity to put your skills to work in clinical research.
\n
\nOur Lincoln, NE location is hiring multiple Lab Technicians / Bioanalytical Associate Analysts to join our team. These roles are Full-time, benefited positions. Salary starts at $20.50 per hour and is commensurate with experience, with opportunities for an increase at 6-9 months with successful performance and attendance.
\n
\nWe are only considering candidates who currently live in the Lincoln, NE area and are ready to begin work in the next 4 weeks.
\n
\nResponsibilities:
\n\n- Process/extract biological samples (blood, urine, plasma, feces) both manually and using automation
\n- Prepare solutions/reagents
\n- Record and document test data in notebooks/binders/electronic notebooks
\n- Perform analytical analysis of samples using chromatography (LC-MS/MS and HPLC) or ligand-binding techniques (ELISA, RIA, EIA and PCR)
\n
\n
\nQualifications:
\n\n
\n- Associate’s degree, Bachelor's degree or previous coursework in Microbiology, Chemistry, Biochemistry, Biology or a related field is preferred
\n- Exposure to pipetting; will pipette an average of 2-3 hours per day, at times up to 8 hours
\n- Experience with GLP’s is a plus
\n- Basic computer skills; able to read and enter information via computer 50% of the shift
\n- Strong attention to detail and self-motivation
\n
\n
\n
Shift:
\n
\n- Monday - Friday daily, during normal business hours, 8am-5pm, with some flexibility
\n- Due to the highly variable nature of our business, we ask you to be available for at least 1 weekend day a month
\n- Flexibility for occasional evening and weekend support
\n
\n
Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
","openingPlain":"Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. \n","descriptionBody":"Do you have basic knowledge of Chromatography or Ligand-Binding techniques and laboratory experience? If so, this could be the position for you! This is a great opportunity to put your skills to work in clinical research.
\n
\nOur Lincoln, NE location is hiring multiple Lab Technicians / Bioanalytical Associate Analysts to join our team. These roles are Full-time, benefited positions. Salary starts at $20.50 per hour and is commensurate with experience, with opportunities for an increase at 6-9 months with successful performance and attendance.
\n
\nWe are only considering candidates who currently live in the Lincoln, NE area and are ready to begin work in the next 4 weeks.
\n
\nResponsibilities:
\n\n- Process/extract biological samples (blood, urine, plasma, feces) both manually and using automation
\n- Prepare solutions/reagents
\n- Record and document test data in notebooks/binders/electronic notebooks
\n- Perform analytical analysis of samples using chromatography (LC-MS/MS and HPLC) or ligand-binding techniques (ELISA, RIA, EIA and PCR)
\n
\n
\nQualifications:
\n\n
\n- Associate’s degree, Bachelor's degree or previous coursework in Microbiology, Chemistry, Biochemistry, Biology or a related field is preferred
\n- Exposure to pipetting; will pipette an average of 2-3 hours per day, at times up to 8 hours
\n- Experience with GLP’s is a plus
\n- Basic computer skills; able to read and enter information via computer 50% of the shift
\n- Strong attention to detail and self-motivation
\n
\n
\n
Shift:
\n
\n- Monday - Friday daily, during normal business hours, 8am-5pm, with some flexibility
\n- Due to the highly variable nature of our business, we ask you to be available for at least 1 weekend day a month
\n- Flexibility for occasional evening and weekend support
\n
\n
Celerion Values: Integrity Trust Teamwork Respect
\n
\nCelerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.
\n
\n\n
Note: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as \"Not Junk\" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.
\n
\n
Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
\n
Bring your cellular biology experience into a hands-on clinical research environment where accuracy, adaptability, and strong lab technique matter every day.
\n
Celerion’s Lincoln, NE location is hiring a part-time Lab Technician / Associate Analyst to join our Molecular and Cellular Biology team. This role is ideal for someone with experience with sterile technique, strong pipetting skills, and a flexible schedule that can adapt as business needs change.
\n
In this role, you will support biological sample processing, reagent preparation, analytical testing, and data documentation in a fast-paced lab setting. As you gain independence over your first 3–6 months, your schedule will become more variable to support evening and weekend shifts. If your life outside work allows you to say \"yes\" when the schedule shifts, you'll thrive in this role.
\n
Why this role may be a strong fit
\n
This is a good opportunity for someone who wants to:
\n
\n- Build deeper hands-on experience in a clinical research laboratory
\n- Work with biological samples including blood, urine, plasma, and feces
\n- Use molecular and cellular biology techniques in a regulated environment
\n- Grow their independence over time while supporting meaningful research
\n- Work part-time hours with the understanding that schedule flexibility is essential
\n
\n
What to expect:
\n
\n- Starting wage: $20.50/hour with performance-based increases over time
\n- Training period: ~30 hours/week for 4-5 weeks
\n- Post-training: ~20 hours/week — but your schedule will vary, and flexibility is essential
\n- Scheduling: Minimum 1-week notice provided; occasional extra shifts may be requested
\n- Benefits: This is a non-benefited position
\n- Location: Local candidates only
\n
\n
Responsibilities:
\n
\n- Process and extract biological samples (blood, urine, plasma, feces) manually and via automation
\n- Prepare solutions and reagents
\n- Record and document test data in notebooks and electronic systems
\n- Support PBMC harvesting and processing
\n- Perform analytical analysis to support flow cytometry and PCR analysis
\n- Maintain strong attention to detail while completing repetitive, precise laboratory tasks
\n
\n
Qualifications:
\n
\n- Associate's or Bachelor's degree — or 2+ years of coursework — in Microbiology, Chemistry, Biochemistry, Biology, or a related field
\n- Experience with sterile technique working in a biosafety cabinet.
\n- Strong pipetting experience; expect 2–3 hours of pipetting daily, occasionally up to 8 hours
\n- Basic computer skills; data entry comprises ~50% of each shift
\n- GLP experience is a plus
\n- Strong attention to detail and self-motivation
\n
\n
Important note about availability:
\n
\n- Because this role supports a dynamic clinical research environment, candidates with limited or fixed availability may not be the right fit at this time. This position is best suited for someone who can say “yes” when the schedule shifts and who is comfortable with variability as part of the role.
\n
\n
Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
","openingPlain":"Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. \n","descriptionBody":"\n
Bring your cellular biology experience into a hands-on clinical research environment where accuracy, adaptability, and strong lab technique matter every day.
\n
Celerion’s Lincoln, NE location is hiring a part-time Lab Technician / Associate Analyst to join our Molecular and Cellular Biology team. This role is ideal for someone with experience with sterile technique, strong pipetting skills, and a flexible schedule that can adapt as business needs change.
\n
In this role, you will support biological sample processing, reagent preparation, analytical testing, and data documentation in a fast-paced lab setting. As you gain independence over your first 3–6 months, your schedule will become more variable to support evening and weekend shifts. If your life outside work allows you to say \"yes\" when the schedule shifts, you'll thrive in this role.
\n
Why this role may be a strong fit
\n
This is a good opportunity for someone who wants to:
\n
\n- Build deeper hands-on experience in a clinical research laboratory
\n- Work with biological samples including blood, urine, plasma, and feces
\n- Use molecular and cellular biology techniques in a regulated environment
\n- Grow their independence over time while supporting meaningful research
\n- Work part-time hours with the understanding that schedule flexibility is essential
\n
\n
What to expect:
\n
\n- Starting wage: $20.50/hour with performance-based increases over time
\n- Training period: ~30 hours/week for 4-5 weeks
\n- Post-training: ~20 hours/week — but your schedule will vary, and flexibility is essential
\n- Scheduling: Minimum 1-week notice provided; occasional extra shifts may be requested
\n- Benefits: This is a non-benefited position
\n- Location: Local candidates only
\n
\n
Responsibilities:
\n
\n- Process and extract biological samples (blood, urine, plasma, feces) manually and via automation
\n- Prepare solutions and reagents
\n- Record and document test data in notebooks and electronic systems
\n- Support PBMC harvesting and processing
\n- Perform analytical analysis to support flow cytometry and PCR analysis
\n- Maintain strong attention to detail while completing repetitive, precise laboratory tasks
\n
\n
Qualifications:
\n
\n- Associate's or Bachelor's degree — or 2+ years of coursework — in Microbiology, Chemistry, Biochemistry, Biology, or a related field
\n- Experience with sterile technique working in a biosafety cabinet.
\n- Strong pipetting experience; expect 2–3 hours of pipetting daily, occasionally up to 8 hours
\n- Basic computer skills; data entry comprises ~50% of each shift
\n- GLP experience is a plus
\n- Strong attention to detail and self-motivation
\n
\n
Important note about availability:
\n
\n- Because this role supports a dynamic clinical research environment, candidates with limited or fixed availability may not be the right fit at this time. This position is best suited for someone who can say “yes” when the schedule shifts and who is comfortable with variability as part of the role.
\n
\n
If this role is what you are looking for as the next step in your career, then please apply!
Celerion Values: Integrity Trust Teamwork Respect
\n
\nCelerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.
\n
\n\n
Note: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as \"Not Junk\" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.
\n
\n
Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
Are you a Bioanalytical Quality Professional with experience in quality assurance and team management looking to make an impact in a dynamic clinical research environment?
\n
\nAt Celerion, we're transforming clinical research through translational medicine. We're seeking a talented Manager/Senior Manager, Quality Assurance, Bioanalytical for our Global QA department to drive quality and compliance of our studies, processes and systems which is key to our mission of accelerating medicine for patients.
\n
\nIdeally this role would be locally based at our Lincoln, Nebraska US location or alternatively at our Tempe, Arizona US location. Hybrid working and willingness to travel from other locations in the United States would also be considered.
","id":"9ccfd727-f532-461c-8fb2-fd006bafaf94","lists":[{"text":"What You’ll Do: ","content":"\nQA Bioanalytical Team Direction and Management\nDriving QMS and Process Improvement Initiatives\nOversight of Study Audits, System/Process Audits and Vendor Audits\nHosting Sponsor Audits and Regulatory Inspections\nActively contributing to Global QA Strategy\n"},{"text":"What You’ll Bring:","content":"\nAbility to communicate and interact at all levels within multicultural environment\nAbility to organize and manage multiple priorities\nStrong problem solving, comprehension and analytical skills\nCollaborative team player, open minded, ethical and culturally sensitive\nAbility to manage and resolve conflict\nGood, well-developed leadership skills\nExcellent written and oral communication skills\nAttention to detail, tactful and diplomatic\nAdvanced Computer skills and literacy\n"},{"text":"What is Required:","content":"\nBachelor’s degree in Business, Science, or related field or equivalent experience\nMinimum of 8 to 10 years experience in Quality Assurance\nMinimum of 4 to 5 years team management experience\nProficient knowledge of GXP (specifically GLP and/or GCP) and FDA 21 CFR Part 11 regulations\nRobust knowledge of Bioanalytical techniques, regulations and industry guidelines\nWell-developed Pharmaceutical Industry network\n"}],"text":"Manager/Senior Manager, Quality Assurance, Bioanalytical","country":"US","workplaceType":"onsite","opening":"Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
","openingPlain":"Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. \n","descriptionBody":"Are you a Bioanalytical Quality Professional with experience in quality assurance and team management looking to make an impact in a dynamic clinical research environment?
\n
\nAt Celerion, we're transforming clinical research through translational medicine. We're seeking a talented Manager/Senior Manager, Quality Assurance, Bioanalytical for our Global QA department to drive quality and compliance of our studies, processes and systems which is key to our mission of accelerating medicine for patients.
\n
\nIdeally this role would be locally based at our Lincoln, Nebraska US location or alternatively at our Tempe, Arizona US location. Hybrid working and willingness to travel from other locations in the United States would also be considered.
","descriptionBodyPlain":"Are you a Bioanalytical Quality Professional with experience in quality assurance and team management looking to make an impact in a dynamic clinical research environment?\n \nAt Celerion, we're transforming clinical research through translational medicine. We're seeking a talented Manager/Senior Manager, Quality Assurance, Bioanalytical for our Global QA department to drive quality and compliance of our studies, processes and systems which is key to our mission of accelerating medicine for patients.\n \nIdeally this role would be locally based at our Lincoln, Nebraska US location or alternatively at our Tempe, Arizona US location. Hybrid working and willingness to travel from other locations in the United States would also be considered. \n","hostedUrl":"https://jobs.lever.co/celerion/9ccfd727-f532-461c-8fb2-fd006bafaf94","applyUrl":"https://jobs.lever.co/celerion/9ccfd727-f532-461c-8fb2-fd006bafaf94/apply"},{"additionalPlain":"This is a part-time, role that will work 20-25 hours per week. Preferred availability for this role includes early weekday morning from 6a-10a. Weekend availability is also required. Pay starting at $17.50/hour.\n \nIf you are a Gmail user and you chose to receive e-mails from @celerion.com, please check your Spam folder regarding the status of your application, including requests for availability and interview invitations. Additionally, ensure you mark Celerion e-mails as “Not Junk”.\n\n\nCelerion Values: Integrity Trust Teamwork Respect\n \nCelerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.\n \nNote: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as \"Not Junk\" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.\n \n","additional":"This is a part-time, role that will work 20-25 hours per week. Preferred availability for this role includes early weekday morning from 6a-10a. Weekend availability is also required. Pay starting at $17.50/hour.
\n
\nIf you are a Gmail user and you chose to receive e-mails from @celerion.com, please check your Spam folder regarding the status of your application, including requests for availability and interview invitations. Additionally, ensure you mark Celerion e-mails as “Not Junk”.
Celerion Values: Integrity Trust Teamwork Respect
\n
\nCelerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.
\n
\n\n
Note: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as \"Not Junk\" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.
\n
\n
Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
Are you looking for an opportunity to support a business creating life-saving treatments? If so, we can't wait to meet you!
\n
\nMedical Research Assistants will monitor activities of study participants, handle human biological samples and record data. Responsibilities also include taking vital signs, performing EKGs, phlebotomy, height/weight, and monitoring meals. Excellent training is provided. Previous medical experience is preferred, but not required.
","id":"8d15f484-04ed-443b-9e03-86ea9645552e","lists":[{"text":"Knowledge/Skills/Education/Licenses:","content":"\nHigh school diploma or GED\nPost high school education in life sciences or medical training preferred\nCPR certification preferred\nExperience in accurate documentation of data preferred\n"}],"salaryRange":{"currency":"USD","interval":"per-hour-wage","min":17.5,"max":17.5},"text":"Medical Research Assistant (part time weekday mornings)","country":"US","workplaceType":"onsite","opening":"Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
","openingPlain":"Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. \n","descriptionBody":"Are you looking for an opportunity to support a business creating life-saving treatments? If so, we can't wait to meet you!
\n
\nMedical Research Assistants will monitor activities of study participants, handle human biological samples and record data. Responsibilities also include taking vital signs, performing EKGs, phlebotomy, height/weight, and monitoring meals. Excellent training is provided. Previous medical experience is preferred, but not required.
","descriptionBodyPlain":"Are you looking for an opportunity to support a business creating life-saving treatments? If so, we can't wait to meet you!\n \nMedical Research Assistants will monitor activities of study participants, handle human biological samples and record data. Responsibilities also include taking vital signs, performing EKGs, phlebotomy, height/weight, and monitoring meals. Excellent training is provided. Previous medical experience is preferred, but not required.\n","hostedUrl":"https://jobs.lever.co/celerion/8d15f484-04ed-443b-9e03-86ea9645552e","applyUrl":"https://jobs.lever.co/celerion/8d15f484-04ed-443b-9e03-86ea9645552e/apply"},{"additionalPlain":"Celerion Values: Integrity Trust Teamwork Respect\n \nCelerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.\n \nNote: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as \"Not Junk\" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.\n \n","additional":"Celerion Values: Integrity Trust Teamwork Respect
\n
\nCelerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.
\n
\n\n
Note: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as \"Not Junk\" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.
\n
\n
Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
We are searching for a full-time Medical Writer to work remotely. This position will analyze and interpret safety results of clinical trials. Compile, write and edit clinical study reports and other industry documents. Confirm accurate classification of events and medications using standardized coding systems.
","id":"a1d7ecaa-ae21-413f-82f0-d76619031d7a","lists":[{"text":"Responsibilities","content":"\nAnalyze and interpret all types of medical results including, but not limited to the following: vital signs, clinical laboratory values, adverse events, electrocardiograms (ECGs), diagnostic procedures, and various pharmacodynamic (PD) endpoints.Compile and write Phase I and Phase II clinical trial documents including, but not limited to the following: clinical study reports (CSRs), stand-alone safety narratives, and synoptic CSRs.\nReview/evaluate study results to determine whether or not the safety objectives and/or endpoints were met, accurately reflecting the results in the safety text. \n Perform peer QC function of safety text prior to inclusion in the CSR.Review reports for completeness and accuracy assuring that the safety text fits into the CSR as whole and recommending changes or rewriting, as appropriate.\nAs the project Report Lead on a multi-disciplinary scientific team, ensoure quality and on-time delivery of scientific reports.\nMonitor content of editorial comments received prior to incorporation into the report to assure report text comments are accurate and support the objectives and/or endpoints.\nAssure deliverables are compliant with applicable regulatory standards (i.e. Good Clinical Practice, International Conference on Harmonisation guidelines) and client specifications.\nUse technology to work with international teams (e.g., WebEx™,Veeva, Microsoft® 365 applications, SharePoint®, and SmartSheet).\nLead-Project-related client communication\nInteract with internal departments (e.g. data management, project management, business development, etc.).\n Participate in functions required to ensure success of department and/or market segment team.\n"},{"text":"Requirements","content":"\nBachelor's degree and/or professional license in a medical or scientific field (RN, BS, RPh, MS, MPH) required or equivalent experience.\n1-3 years experience in hospital/clinical setting or interpreting medical or clinical results.\nProfessional writing and editing skills for accurate and concise reporting of clinical trial results; ability to interpret and present data in preparing a coherently written document.\nDetail-oriented, thorough, and methodical.\nAbility to work without close supervision and ability to work under pressure.\nAbility to multi-task and to respond rapidly to changing priorities and aggressive timelines.\nExcellent communication/ interpersonal skills.\nKnowledge of medical, pharmaceutical, and/or clinical research concepts preferred. \n"}],"text":"Medical Writer","country":"US","workplaceType":"remote","opening":"Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
","openingPlain":"Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. \n","descriptionBody":"We are searching for a full-time Medical Writer to work remotely. This position will analyze and interpret safety results of clinical trials. Compile, write and edit clinical study reports and other industry documents. Confirm accurate classification of events and medications using standardized coding systems.
","descriptionBodyPlain":"We are searching for a full-time Medical Writer to work remotely. This position will analyze and interpret safety results of clinical trials. Compile, write and edit clinical study reports and other industry documents. Confirm accurate classification of events and medications using standardized coding systems.\n","hostedUrl":"https://jobs.lever.co/celerion/a1d7ecaa-ae21-413f-82f0-d76619031d7a","applyUrl":"https://jobs.lever.co/celerion/a1d7ecaa-ae21-413f-82f0-d76619031d7a/apply"},{"additional":"","additionalPlain":"","categories":{"commitment":"Full-Time","department":"4112 - Bioanalytical Services","location":"Fehraltorf (Zurich), Switzerland","team":"4112 - Bioanalytical Services","allLocations":["Fehraltorf (Zurich), Switzerland"]},"createdAt":1786113965965,"descriptionPlain":"Celerion ist eines der weltweit führenden Unternehmen der bioanalytischen Auftragsforschung und unterstützt seit mehr als 40 Jahren Pharma- und Biotechfirmen auf der ganzen Welt. Celerion bietet Dienstleistungen für die Zulassung von neuen Medikamenten - von frühen Entwicklungsarbeiten bis hin zu klinischen Studien mit dem Ziel, Patienten möglichst schnell zu helfen.\n \nAufgrund des stetigen Wachstums unseres Unternehmens und zur Verstärkung unserer Daten- und Berichtskontrolle innerhalb unserer Bioanalytik suchen wir eine engagierte Persönlichkeit als\n \n \nMitarbeiter/in Quality Control 80-100%\n \nIhr Aufgabengebiet\nÜberprüfung von Rohdaten, die während einer bioanalytischen Studie generiert werden\nKontrolle von weiterführenden Daten und Studienresultaten \nÜberprüfung von Berichten am Ende einer Studie\nAls Teil des QC Teams übernehmen Sie nach sorgfältiger Einarbeitung eigene Aufgaben.\n \nIhr Profil\nBachelor Biologie / (Bio-) Chemie oder Ausbildung als Chemie- oder Biologielaborant/in, CTA, BTA oder MTA\nTeam-player, verlässlich, genau, hochmotiviert, gute Selbstorganisation\nFachkenntnisse im Bereich LBA oder LC-MS/MS\ngute Deutsch- und Englischkenntnisse\nBerufserfahrung in einem regulierten Umfeld (GxP/ISO)\nFreude an einem Office-basierten Job\n \nWir bieten\nInteressante Tätigkeit in einem offenen, dynamischen Team\n„On the job“ Weiterbildung und Entwicklung\nModerne Infrastruktur\nWork-Life-Balance: flexible Arbeitszeiten (Mo bis Fr, keine Wochenenden, keine Schicht,), mind. 5 Wochen Ferien\nFinanzielles: Lohngleichheit zwischen den Geschlechtern, sehr gute Sozialleistungen, Bezug von REKA-Checks\n","description":"\n
Celerion ist eines der weltweit führenden Unternehmen der bioanalytischen Auftragsforschung und unterstützt seit mehr als 40 Jahren Pharma- und Biotechfirmen auf der ganzen Welt. Celerion bietet Dienstleistungen für die Zulassung von neuen Medikamenten - von frühen Entwicklungsarbeiten bis hin zu klinischen Studien mit dem Ziel, Patienten möglichst schnell zu helfen.
\n
\n
Aufgrund des stetigen Wachstums unseres Unternehmens und zur Verstärkung unserer Daten- und Berichtskontrolle innerhalb unserer Bioanalytik suchen wir eine engagierte Persönlichkeit als
\n
\n
\n
Mitarbeiter/in Quality Control 80-100%
\n
\n
Ihr Aufgabengebiet
\n
\n- Überprüfung von Rohdaten, die während einer bioanalytischen Studie generiert werden
\n- Kontrolle von weiterführenden Daten und Studienresultaten
\n- Überprüfung von Berichten am Ende einer Studie
\n
\n
Als Teil des QC Teams übernehmen Sie nach sorgfältiger Einarbeitung eigene Aufgaben.
\n
\n
Ihr Profil
\n
\n- Bachelor Biologie / (Bio-) Chemie oder Ausbildung als Chemie- oder Biologielaborant/in, CTA, BTA oder MTA
\n
\n
\n- Team-player, verlässlich, genau, hochmotiviert, gute Selbstorganisation
\n
\n
\n- Fachkenntnisse im Bereich LBA oder LC-MS/MS
\n- gute Deutsch- und Englischkenntnisse
\n
\n
\n- Berufserfahrung in einem regulierten Umfeld (GxP/ISO)
\n
\n
\n- Freude an einem Office-basierten Job
\n
\n
\n
Wir bieten
\n
\n- Interessante Tätigkeit in einem offenen, dynamischen Team
\n- „On the job“ Weiterbildung und Entwicklung
\n- Moderne Infrastruktur
\n- Work-Life-Balance: flexible Arbeitszeiten (Mo bis Fr, keine Wochenenden, keine Schicht,), mind. 5 Wochen Ferien
\n- Finanzielles: Lohngleichheit zwischen den Geschlechtern, sehr gute Sozialleistungen, Bezug von REKA-Checks
\n
\n
\n
Celerion ist eines der weltweit führenden Unternehmen der bioanalytischen Auftragsforschung und unterstützt seit mehr als 40 Jahren Pharma- und Biotechfirmen auf der ganzen Welt. Celerion bietet Dienstleistungen für die Zulassung von neuen Medikamenten - von frühen Entwicklungsarbeiten bis hin zu klinischen Studien mit dem Ziel, Patienten möglichst schnell zu helfen.
\n
\n
Aufgrund des stetigen Wachstums unseres Unternehmens und zur Verstärkung unserer Daten- und Berichtskontrolle innerhalb unserer Bioanalytik suchen wir eine engagierte Persönlichkeit als
\n
\n
\n
Mitarbeiter/in Quality Control 80-100%
\n
\n
Ihr Aufgabengebiet
\n
\n- Überprüfung von Rohdaten, die während einer bioanalytischen Studie generiert werden
\n- Kontrolle von weiterführenden Daten und Studienresultaten
\n- Überprüfung von Berichten am Ende einer Studie
\n
\n
Als Teil des QC Teams übernehmen Sie nach sorgfältiger Einarbeitung eigene Aufgaben.
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Ihr Profil
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\n- Bachelor Biologie / (Bio-) Chemie oder Ausbildung als Chemie- oder Biologielaborant/in, CTA, BTA oder MTA
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\n- Team-player, verlässlich, genau, hochmotiviert, gute Selbstorganisation
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\n- Fachkenntnisse im Bereich LBA oder LC-MS/MS
\n- gute Deutsch- und Englischkenntnisse
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\n- Berufserfahrung in einem regulierten Umfeld (GxP/ISO)
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\n- Freude an einem Office-basierten Job
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Wir bieten
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\n- Interessante Tätigkeit in einem offenen, dynamischen Team
\n- „On the job“ Weiterbildung und Entwicklung
\n- Moderne Infrastruktur
\n- Work-Life-Balance: flexible Arbeitszeiten (Mo bis Fr, keine Wochenenden, keine Schicht,), mind. 5 Wochen Ferien
\n- Finanzielles: Lohngleichheit zwischen den Geschlechtern, sehr gute Sozialleistungen, Bezug von REKA-Checks
\n
\n
Why Celerion?
\nAt Celerion, your work as an IT Specialist is not just about keeping computers running — it is about enabling the scientists and clinicians who are accelerating the journey from laboratory to patient. You will be part of a global, collaborative IT team with the support and resources of an established international organization, while enjoying the close-knit atmosphere of our Swiss site.
","categories":{"commitment":"Full-Time","department":"Job Posting Categories","location":"Fehraltorf (Zurich), Switzerland","team":"Information Technology","allLocations":["Fehraltorf (Zurich), Switzerland"]},"createdAt":1773340816737,"descriptionPlain":"For over 40 years, Celerion has stood at the forefront of global bioanalytical contract research, partnering with pharmaceutical and biotech innovators to bring new therapies to patients faster. Our growing Fehraltorf/Zurich site is at the heart of that mission.\nTHE OPPORTUNITY\nWe are looking for a technically versatile and people-oriented On- Site IT Specialist to join our global IT team in Zurich. As one of the primary on-site IT representatives, you will serve as the trusted face of IT for our Swiss colleagues — combining deep technical skills with genuine service commitment. If you thrive on solving complex problems and want your expertise to matter, this role is for you.\n","description":"For over 40 years, Celerion has stood at the forefront of global bioanalytical contract research, partnering with pharmaceutical and biotech innovators to bring new therapies to patients faster. Our growing Fehraltorf/Zurich site is at the heart of that mission.
\nTHE OPPORTUNITY
\nWe are looking for a technically versatile and people-oriented On- Site IT Specialist to join our global IT team in Zurich. As one of the primary on-site IT representatives, you will serve as the trusted face of IT for our Swiss colleagues — combining deep technical skills with genuine service commitment. If you thrive on solving complex problems and want your expertise to matter, this role is for you.
","id":"fd40152f-09f6-4bd1-9a3f-b1163fb08415","lists":[{"text":"Key Responsibilities:","content":"\n
\n- Serve as a primary on-site IT point of contact and escalation lead for the Zurich site, coordinating with local and global IT teams as needed.
\n- Deliver comprehensive desktop and systems support across Microsoft operating systems, Microsoft 365, Adobe Acrobat/Creative Cloud, Oracle Client Tools, Citrix Virtual Apps and Desktop, and Microsoft Defender for Endpoint.
\n- Execute Install/Move/Add/Change (IMAC) activities and perform preventative maintenance to ensure optimal workstation performance.
\n- Provide hands-on support for Windows Server environments, Active Directory, and local network infrastructure — including switches, patch panels, and structured cabling — in coordination with centralized infrastructure teams.
\n- Manage and resolve daily support activities via the ticket management system, maintaining accurate updates and clear user communication through to resolution.
\n- Support local backup, restore, and archival processes; maintain working knowledge of ODBC connectivity and basic SQL client configuration.
\n- Lead endpoint deployment and imaging activities using tools such as Microsoft Intune, SCCM/MECM, and Autopilot.
\n- Ensure all endpoint and infrastructure systems comply with GxP and data-integrity regulatory requirements, validated processes, and change control procedures.
\n- Provide IT onboarding training for new hires and ongoing end-user guidance to maximize productivity.
\n- Assist with on-site cabling, local switch installation, and network equipment troubleshooting.
\n\n
For over 40 years, Celerion has stood at the forefront of global bioanalytical contract research, partnering with pharmaceutical and biotech innovators to bring new therapies to patients faster. Our growing Fehraltorf/Zurich site is at the heart of that mission.
\nTHE OPPORTUNITY
\nWe are looking for a technically versatile and people-oriented On- Site IT Specialist to join our global IT team in Zurich. As one of the primary on-site IT representatives, you will serve as the trusted face of IT for our Swiss colleagues — combining deep technical skills with genuine service commitment. If you thrive on solving complex problems and want your expertise to matter, this role is for you.
","descriptionBodyPlain":"For over 40 years, Celerion has stood at the forefront of global bioanalytical contract research, partnering with pharmaceutical and biotech innovators to bring new therapies to patients faster. Our growing Fehraltorf/Zurich site is at the heart of that mission.\nTHE OPPORTUNITY\nWe are looking for a technically versatile and people-oriented On- Site IT Specialist to join our global IT team in Zurich. As one of the primary on-site IT representatives, you will serve as the trusted face of IT for our Swiss colleagues — combining deep technical skills with genuine service commitment. If you thrive on solving complex problems and want your expertise to matter, this role is for you.\n","hostedUrl":"https://jobs.lever.co/celerion/fd40152f-09f6-4bd1-9a3f-b1163fb08415","applyUrl":"https://jobs.lever.co/celerion/fd40152f-09f6-4bd1-9a3f-b1163fb08415/apply"},{"additionalPlain":"Celerion Values: Integrity Trust Teamwork Respect\n \nAre you ready to join our team?\n \nCelerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.\n \nNote: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as \"Not Junk\" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.\n \n","additional":"Celerion Values: Integrity Trust Teamwork Respect
\n
\nAre you ready to join our team?
\n
\nCelerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.
\n
\n\n
Note: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as \"Not Junk\" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.
\n
\n
Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
Job Purpose
\n
\nThe Participant Care Specialist is responsible for assessing, planning, facilitating and advocating for options and services directed to enhance participants’ experiences from initial point of contact at screening through study completion. This role will focus on providing customer service and interacting with participants directly in order to obtain data related to the participants’ experience.
","id":"1ae28d19-e2a2-478c-9fc3-f31fad59491e","lists":[{"text":"Essential Functions","content":"\nResponsible for and manages the participant experience during all phases of a clinical study (screening, conduct, post study follow-up)\nAct as the point person in the clinic to handle participant questions, complaints and resolving participant related issue escalations\nDevelop, track and respond to participant survey feedback and make recommendations for improvement\nCreate, plan and oversee participant activities during conduct\nParticipate in the Participant Care Committee to make decisions that enhance the participant experience within Celerion\nProactively identifies new needs or capabilities to enhance participant satisfaction\nKeep participants informed of study information\nDirect staff based on participant care priorities. Redirect and provide feedback for improved participant interactions as needed. (Using CARE and AIDET standards).\nCollaborate with managers regarding participant orientation sessions, clinical tours, screening process flow, alternate releases, etc.\nAbility to work in required work environment, including but not limited to working in a clinical/ laboratory environment with exposure to biological/ biohazardous materials.\nConduct other reasonable duties as assigned \n"},{"text":"Knowledge/Skills/Education/Licenses","content":"\nExcellent customer service skills with 2 years customer service experience\nExcellent oral and written communication skills\nBilingual in English and Spanish required \nExcellent interpersonal skills\nFlexibility to work evening, weekend and flexible hours as needed.\nAbility to manage multiple priorities in a fast–paced environment.\nExcellent organizational and problem-solving skills.\nEquivalent education and experience will be considered.\nSchedule: Monday - Friday (Flexible - 7 AM - 4 PM), Occasional weekend availability\n"}],"salaryRange":{"min":22,"currency":"USD","interval":"per-hour-wage","max":22},"text":"Participant Care Specialist - Spanish Bilingual","country":"US","workplaceType":"onsite","opening":"Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
","openingPlain":"Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. \n","descriptionBody":"Job Purpose
\n
\nThe Participant Care Specialist is responsible for assessing, planning, facilitating and advocating for options and services directed to enhance participants’ experiences from initial point of contact at screening through study completion. This role will focus on providing customer service and interacting with participants directly in order to obtain data related to the participants’ experience.
","descriptionBodyPlain":"Job Purpose \n\nThe Participant Care Specialist is responsible for assessing, planning, facilitating and advocating for options and services directed to enhance participants’ experiences from initial point of contact at screening through study completion. This role will focus on providing customer service and interacting with participants directly in order to obtain data related to the participants’ experience. \n","hostedUrl":"https://jobs.lever.co/celerion/1ae28d19-e2a2-478c-9fc3-f31fad59491e","applyUrl":"https://jobs.lever.co/celerion/1ae28d19-e2a2-478c-9fc3-f31fad59491e/apply"},{"additionalPlain":"Celerion Values: Integrity Trust Teamwork Respect\n \nCelerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.\n \nNote: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as \"Not Junk\" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.\n \n","additional":"Celerion Values: Integrity Trust Teamwork Respect
\n
\nCelerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.
\n
\n\n
Note: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as \"Not Junk\" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.
\n
\n
Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
In this position, you will be assisting in pharmacy functions, including receipt, packaging, and retention of clinical samples. This position is full time and we are looking for an individual with availability to work between 8:00 am - 5:00 pm weekdays; with rotating weekend on-call, occasional early morning and weekend hours.
\n
\nRequirements
\nWe require a high school diploma or GED and prefer post high school education in life sciences or medical training. This individual must have strong attention to detail and the ability to work a flexible schedule. We also prefer a candidate with knowledge of FDA/controlled substance laws and general computer skills including Microsoft Word and Excel. Another skill required is hospital/compounding experience.
","id":"6bab76f8-5aca-40cb-be3b-bb48544ba70e","lists":[],"salaryRange":{"min":20,"max":22,"currency":"USD","interval":"per-hour-wage"},"text":"Pharmacy Technician - Full-Time - Lincoln, Nebraska","country":"US","workplaceType":"onsite","opening":"Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
","openingPlain":"Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. \n","descriptionBody":"In this position, you will be assisting in pharmacy functions, including receipt, packaging, and retention of clinical samples. This position is full time and we are looking for an individual with availability to work between 8:00 am - 5:00 pm weekdays; with rotating weekend on-call, occasional early morning and weekend hours.
\n
\nRequirements
\nWe require a high school diploma or GED and prefer post high school education in life sciences or medical training. This individual must have strong attention to detail and the ability to work a flexible schedule. We also prefer a candidate with knowledge of FDA/controlled substance laws and general computer skills including Microsoft Word and Excel. Another skill required is hospital/compounding experience.
","descriptionBodyPlain":"In this position, you will be assisting in pharmacy functions, including receipt, packaging, and retention of clinical samples. This position is full time and we are looking for an individual with availability to work between 8:00 am - 5:00 pm weekdays; with rotating weekend on-call, occasional early morning and weekend hours. \n \nRequirements\nWe require a high school diploma or GED and prefer post high school education in life sciences or medical training. This individual must have strong attention to detail and the ability to work a flexible schedule. We also prefer a candidate with knowledge of FDA/controlled substance laws and general computer skills including Microsoft Word and Excel. Another skill required is hospital/compounding experience.\n","hostedUrl":"https://jobs.lever.co/celerion/6bab76f8-5aca-40cb-be3b-bb48544ba70e","applyUrl":"https://jobs.lever.co/celerion/6bab76f8-5aca-40cb-be3b-bb48544ba70e/apply"},{"additionalPlain":"If you are a Gmail user and you chose to receive e-mails from @celerion.com, please check your Spam folder regarding the status of your application, including requests for availability and interview invitations. Additionally, ensure you mark Celerion e-mails as “Not Junk”.\n\n\nCelerion Values: Integrity Trust Teamwork Respect\n \nCelerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.\n \nNote: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as \"Not Junk\" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.\n \n","additional":"If you are a Gmail user and you chose to receive e-mails from @celerion.com, please check your Spam folder regarding the status of your application, including requests for availability and interview invitations. Additionally, ensure you mark Celerion e-mails as “Not Junk”.
Celerion Values: Integrity Trust Teamwork Respect
\n
\nCelerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.
\n
\n\n
Note: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as \"Not Junk\" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.
\n
\n
Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
The PI is responsible for the safety of subjects who participate in clinical trials and for executing the study according to the IRB-approved protocol and applicable FDA and GCP regulations.
\n
\nPre-Study:
\n· Review protocol and Investigator Brochure for subject safety, scientific, and operational feasibility of study. Provide input to sponsor as indicated.
\n· Complete FDA 1572 and financial disclosure forms.
\n· Attend study initiation meetings with sponsor.
\n· Communicate with Institutional Review Board during protocol approval process and subject safety issues.
\n· Explain study to subject and answer questions, ensure proper consent, and perform screening examination.
\n· Final review of all screening data and authorization of subjects to be enrolled in the study.
\nDuring/Post Study:
\n· Perform scheduled per protocol, and unscheduled per adverse event, physicals during study conduct.
\n· Manage adverse events/clinical evaluation of subjects and determine adverse event relationship to investigational product, severity, and etiology. Review pre-dose lab work, ECGs, and other study data and determine appropriate action plan based on these results. Review safety data with sponsor.
\n· Compose SAE and other reporting documents as indicated.
\n· Review and sign Case Report Forms and final Clinical Study Reports.
\n· Review all serious adverse events and SUSARs to the Sponsor and IRB within statutory timelines
\n· Data review of all end-of-study data to determine if re-checks are necessary
\n· Safety-monitoring – perform end-of-study physical exams and follow-up ongoing adverse events
\n· Case Report Forms review – review and sign all case report forms at end of study
\n· Assist in on-site client review of case report forms
\nAdditional Responsibilities:
\n· Assist with identifying and maintaining a network of physician specialists to contract on studies.
\n· Present Celerion’s capabilities and experience during sponsor meetings and events.
\n· Assist in the design of study and time/event schedules involving special medical procedures
\n· Function as a medical/clinical informational resource for the site.
\n· Assist other departments with development of SOPs, training plans, etc.
\n· Facilitate emergency response training and review of clinical safety procedures.
","id":"d376bf1d-ec02-4bc8-9869-184181b2dbaf","lists":[{"text":"Qualifications","content":"\nMD or DO degree and current state license.\nBasic Life Support and Advanced Cardiac Life Support certification\nSuccessful completion of an ACGME residency program in family medicine, internal medicine, or emergency medicine.\nHold a DEA certificate for schedule II medications\n3-5 years of medical/clinical experience preferred\nClinical research experience preferred\nAble to work a flexible schedule\n"}],"text":"Principal Investigator","country":"US","workplaceType":"onsite","opening":"Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
","openingPlain":"Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. \n","descriptionBody":"The PI is responsible for the safety of subjects who participate in clinical trials and for executing the study according to the IRB-approved protocol and applicable FDA and GCP regulations.
\n
\nPre-Study:
\n· Review protocol and Investigator Brochure for subject safety, scientific, and operational feasibility of study. Provide input to sponsor as indicated.
\n· Complete FDA 1572 and financial disclosure forms.
\n· Attend study initiation meetings with sponsor.
\n· Communicate with Institutional Review Board during protocol approval process and subject safety issues.
\n· Explain study to subject and answer questions, ensure proper consent, and perform screening examination.
\n· Final review of all screening data and authorization of subjects to be enrolled in the study.
\nDuring/Post Study:
\n· Perform scheduled per protocol, and unscheduled per adverse event, physicals during study conduct.
\n· Manage adverse events/clinical evaluation of subjects and determine adverse event relationship to investigational product, severity, and etiology. Review pre-dose lab work, ECGs, and other study data and determine appropriate action plan based on these results. Review safety data with sponsor.
\n· Compose SAE and other reporting documents as indicated.
\n· Review and sign Case Report Forms and final Clinical Study Reports.
\n· Review all serious adverse events and SUSARs to the Sponsor and IRB within statutory timelines
\n· Data review of all end-of-study data to determine if re-checks are necessary
\n· Safety-monitoring – perform end-of-study physical exams and follow-up ongoing adverse events
\n· Case Report Forms review – review and sign all case report forms at end of study
\n· Assist in on-site client review of case report forms
\nAdditional Responsibilities:
\n· Assist with identifying and maintaining a network of physician specialists to contract on studies.
\n· Present Celerion’s capabilities and experience during sponsor meetings and events.
\n· Assist in the design of study and time/event schedules involving special medical procedures
\n· Function as a medical/clinical informational resource for the site.
\n· Assist other departments with development of SOPs, training plans, etc.
\n· Facilitate emergency response training and review of clinical safety procedures.
","descriptionBodyPlain":"The PI is responsible for the safety of subjects who participate in clinical trials and for executing the study according to the IRB-approved protocol and applicable FDA and GCP regulations.\n \nPre-Study: \n· Review protocol and Investigator Brochure for subject safety, scientific, and operational feasibility of study. Provide input to sponsor as indicated.\n· Complete FDA 1572 and financial disclosure forms.\n· Attend study initiation meetings with sponsor.\n· Communicate with Institutional Review Board during protocol approval process and subject safety issues.\n· Explain study to subject and answer questions, ensure proper consent, and perform screening examination.\n· Final review of all screening data and authorization of subjects to be enrolled in the study.\nDuring/Post Study:\n· Perform scheduled per protocol, and unscheduled per adverse event, physicals during study conduct.\n· Manage adverse events/clinical evaluation of subjects and determine adverse event relationship to investigational product, severity, and etiology. Review pre-dose lab work, ECGs, and other study data and determine appropriate action plan based on these results. Review safety data with sponsor.\n· Compose SAE and other reporting documents as indicated.\n· Review and sign Case Report Forms and final Clinical Study Reports.\n· Review all serious adverse events and SUSARs to the Sponsor and IRB within statutory timelines\n· Data review of all end-of-study data to determine if re-checks are necessary\n· Safety-monitoring – perform end-of-study physical exams and follow-up ongoing adverse events\n· Case Report Forms review – review and sign all case report forms at end of study\n· Assist in on-site client review of case report forms\nAdditional Responsibilities: \n· Assist with identifying and maintaining a network of physician specialists to contract on studies.\n· Present Celerion’s capabilities and experience during sponsor meetings and events.\n· Assist in the design of study and time/event schedules involving special medical procedures\n· Function as a medical/clinical informational resource for the site.\n· Assist other departments with development of SOPs, training plans, etc.\n· Facilitate emergency response training and review of clinical safety procedures.\n","hostedUrl":"https://jobs.lever.co/celerion/d376bf1d-ec02-4bc8-9869-184181b2dbaf","applyUrl":"https://jobs.lever.co/celerion/d376bf1d-ec02-4bc8-9869-184181b2dbaf/apply"},{"additionalPlain":"We offer:\n \nA dynamic, groundbreaking and team oriented work environment and a comprehensive benefit package.\n\n\nCelerion Values: Integrity Trust Teamwork Respect\n \nCelerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.\n \nNote: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as \"Not Junk\" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.\n \n","additional":"We offer:
\n
\nA dynamic, groundbreaking and team oriented work environment and a comprehensive benefit package.
Celerion Values: Integrity Trust Teamwork Respect
\n
\nCelerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.
\n
\n\n
Note: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as \"Not Junk\" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.
\n
\n
Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
As a Research Screening Specialist, you will work at our Lincoln, Nebraska site. You will be responsible for the preparation and maintenance of all stages of participant activities including screening, training, and evaluations. Duties include entering and updating study information into database systems, collecting and organizing panelist’s paperwork and documentation, and developing positive participant communications and relationships.
\n
\nIn this entry level role you will work in an office / clinic environment with a team of 10 colleagues all committed to the same mission: assisting in the development of drugs that will touch the lives of family, friends, and people in need around the world.
\nWe prefer an Associate's degree in social or biological sciences or a hospitality related field, excellent oral and written communication skills, excellent organizational skills, and the ability to multi-task effectively.
\n
\nFor this position you may also be required to travel to our Omaha site approximately 1-2 times per week during working hours.
\n
\nThis full time position will work mainly Monday-Friday 5:30am-2:00pm.
\n
\nIf you are seeking a future career in medicine or just want to know more about clinical research, this role is a springboard to professional growth and opportunities for advancement.
\n
","id":"80e8d3dd-ee25-4e07-b8f5-4c6485c1c170","lists":[{"text":"Knowledge / Skills / Education / Licenses:","content":"\nAssociate's degree in related field preferred but not required\nOne year customer services experience\nExperience in organizing and managing multiple priorities\nExcellent oral and written communication skills\nOrganizational skills\nGeneral knowledge of Microsoft Windows based applications\n"}],"salaryRange":{"min":20,"max":20,"currency":"USD","interval":"per-hour-wage"},"text":"Research Screening Specialist - Lincoln, Nebraska","country":"US","workplaceType":"onsite","opening":"Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
","openingPlain":"Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. \n","descriptionBody":"As a Research Screening Specialist, you will work at our Lincoln, Nebraska site. You will be responsible for the preparation and maintenance of all stages of participant activities including screening, training, and evaluations. Duties include entering and updating study information into database systems, collecting and organizing panelist’s paperwork and documentation, and developing positive participant communications and relationships.
\n
\nIn this entry level role you will work in an office / clinic environment with a team of 10 colleagues all committed to the same mission: assisting in the development of drugs that will touch the lives of family, friends, and people in need around the world.
\nWe prefer an Associate's degree in social or biological sciences or a hospitality related field, excellent oral and written communication skills, excellent organizational skills, and the ability to multi-task effectively.
\n
\nFor this position you may also be required to travel to our Omaha site approximately 1-2 times per week during working hours.
\n
\nThis full time position will work mainly Monday-Friday 5:30am-2:00pm.
\n
\nIf you are seeking a future career in medicine or just want to know more about clinical research, this role is a springboard to professional growth and opportunities for advancement.
\n
","descriptionBodyPlain":"As a Research Screening Specialist, you will work at our Lincoln, Nebraska site. You will be responsible for the preparation and maintenance of all stages of participant activities including screening, training, and evaluations. Duties include entering and updating study information into database systems, collecting and organizing panelist’s paperwork and documentation, and developing positive participant communications and relationships. \n \nIn this entry level role you will work in an office / clinic environment with a team of 10 colleagues all committed to the same mission: assisting in the development of drugs that will touch the lives of family, friends, and people in need around the world. \nWe prefer an Associate's degree in social or biological sciences or a hospitality related field, excellent oral and written communication skills, excellent organizational skills, and the ability to multi-task effectively. \n \nFor this position you may also be required to travel to our Omaha site approximately 1-2 times per week during working hours.\n \nThis full time position will work mainly Monday-Friday 5:30am-2:00pm. \n \nIf you are seeking a future career in medicine or just want to know more about clinical research, this role is a springboard to professional growth and opportunities for advancement. \n \n","hostedUrl":"https://jobs.lever.co/celerion/80e8d3dd-ee25-4e07-b8f5-4c6485c1c170","applyUrl":"https://jobs.lever.co/celerion/80e8d3dd-ee25-4e07-b8f5-4c6485c1c170/apply"},{"additionalPlain":"Celerion Values: Integrity Trust Teamwork Respect\n \nCelerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.\n \nNote: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as \"Not Junk\" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.\n \n","additional":"Celerion Values: Integrity Trust Teamwork Respect
\n
\nCelerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.
\n
\n\n
Note: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as \"Not Junk\" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.
\n
\n
Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
Are you looking for an opportunity to support a business creating life-saving treatments? If so, we can't wait to meet you!
\n
\nCelerion is seeking a Scientist to join our Ligand Binding Assay Development team. The successful candidate will have strong problem-solving skills, scientific expertise and knowledge in Ligand Binding bioanalytical method development.
\n
\nThis full-time role is located at our Lincoln, NE facility.
\n
\nAs a Scientist, Method Development, you will provide scientific expertise and method development skills to the Ligand Binding Assay Development group at Celerion. A key component of the role is to provide innovation and change management required to remain on the cutting edge of Ligand Binding Bioanalytical Sciences.
\n
\nResponsibilities:
\n\n
\n- Undertake original and innovative research and techniques that include developing ligand binding assays utilizing state-of-the-art technologies for the rapid and accurate analysis of protein/peptides/ antibodies in biological matrices
\n- Perform assays (pharmacokinetics (PK), pharmacodynamics PD)/biomarkers, ADA) according to regulatory and quality systems
\n- Analyze and interpret data, generate summary tables, and troubleshoot assay performance, as well as peer‑review raw data for accuracy and completeness
\n- Work effectively within a team and across teams to meet objectives under time constraints
\n- Support the associate director in achieving challenging business objectives for the method development team. Includes innovation, change management, evaluation of new technology, and growth in market share, revenue, profit, and customer loyalty.
\n- Develop methods by applying and interpreting scientific theories, concepts, techniques, and regulatory requirements in bioanalytical studies
\n- Provide technical/scientific guidance and leadership to study teams, as well as other areas of the company to ensure project completion in a timely manner
\n- Author scientific manuscripts for publication in peer‑reviewed journals and present research findings through posters and oral presentations at scientific conferences
\n- Participate and provide technical expertise during client calls and visits
\n
\n
Requirements:
\n
\n
\n- Minimum of a Bachelor’s degree in Biochemistry, Chemistry or Biology required. An advanced degree is preferred.
\n- 5+ years of related scientific experience preferred; CRO/industry experience is a plus
\n- The candidate must have proven proficiency in immunoassay development and be capable of working on multiple projects simultaneously
\n- Strong hands-on experience in at least one of the following pharmacokinetics (PK), pharmacodynamics (PD)/biomarkers, ADA assay development
\n- Understanding of FDA and ICH guidelines in method validation and sample analysis
\n- Prior experience working in a regulated GLP-compliant environment is preferred
\n- Experience in one or more immunoassay techniques (Ligand Binding assay: ELISA, MSD, Gyrolab, AlphaLISA)
\n- Experience using Watson LIMS is preferred
\n- Excellent verbal and technical writing skills and be capable of presenting to an audience of researchers from a variety of disciplines
\n- Ability to work well with a team and with staff in other locations effectively
\n
\n
\n
\n
Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
","openingPlain":"Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. \n","descriptionBody":"Are you looking for an opportunity to support a business creating life-saving treatments? If so, we can't wait to meet you!
\n
\nCelerion is seeking a Scientist to join our Ligand Binding Assay Development team. The successful candidate will have strong problem-solving skills, scientific expertise and knowledge in Ligand Binding bioanalytical method development.
\n
\nThis full-time role is located at our Lincoln, NE facility.
\n
\nAs a Scientist, Method Development, you will provide scientific expertise and method development skills to the Ligand Binding Assay Development group at Celerion. A key component of the role is to provide innovation and change management required to remain on the cutting edge of Ligand Binding Bioanalytical Sciences.
\n
\nResponsibilities:
\n\n
\n- Undertake original and innovative research and techniques that include developing ligand binding assays utilizing state-of-the-art technologies for the rapid and accurate analysis of protein/peptides/ antibodies in biological matrices
\n- Perform assays (pharmacokinetics (PK), pharmacodynamics PD)/biomarkers, ADA) according to regulatory and quality systems
\n- Analyze and interpret data, generate summary tables, and troubleshoot assay performance, as well as peer‑review raw data for accuracy and completeness
\n- Work effectively within a team and across teams to meet objectives under time constraints
\n- Support the associate director in achieving challenging business objectives for the method development team. Includes innovation, change management, evaluation of new technology, and growth in market share, revenue, profit, and customer loyalty.
\n- Develop methods by applying and interpreting scientific theories, concepts, techniques, and regulatory requirements in bioanalytical studies
\n- Provide technical/scientific guidance and leadership to study teams, as well as other areas of the company to ensure project completion in a timely manner
\n- Author scientific manuscripts for publication in peer‑reviewed journals and present research findings through posters and oral presentations at scientific conferences
\n- Participate and provide technical expertise during client calls and visits
\n
\n
Requirements:
\n
\n
\n- Minimum of a Bachelor’s degree in Biochemistry, Chemistry or Biology required. An advanced degree is preferred.
\n- 5+ years of related scientific experience preferred; CRO/industry experience is a plus
\n- The candidate must have proven proficiency in immunoassay development and be capable of working on multiple projects simultaneously
\n- Strong hands-on experience in at least one of the following pharmacokinetics (PK), pharmacodynamics (PD)/biomarkers, ADA assay development
\n- Understanding of FDA and ICH guidelines in method validation and sample analysis
\n- Prior experience working in a regulated GLP-compliant environment is preferred
\n- Experience in one or more immunoassay techniques (Ligand Binding assay: ELISA, MSD, Gyrolab, AlphaLISA)
\n- Experience using Watson LIMS is preferred
\n- Excellent verbal and technical writing skills and be capable of presenting to an audience of researchers from a variety of disciplines
\n- Ability to work well with a team and with staff in other locations effectively
\n
\n
\n
\n
Celerion Values: Integrity Trust Teamwork Respect
\n
\nCelerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.
\n
\n\n
Note: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as \"Not Junk\" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.
\n
\n
Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
Celerion is currently seeking a full-time Standard Operating Procedure Designer for our Lincoln, Nebraska location. After 6-8 weeks of on-site training, you will have the ability to work primarily from home, if desired. You will work with your team in person and on-site every other week.
\n
\nIn this position, you will define, develop, implement and maintain Celerion standard processes that adhere to company governance and global regulatory requirements.
","id":"352890af-0c39-4f46-ad21-fc28f763a4a4","lists":[{"text":"Responsibilities:","content":"\nLead global project groups to obtain information needed to create global process documents.\nPlan for and manage reviews of new and existing processes and standards to ensure completeness, consistency, quality and compliance with established requirements.\nManage document control and maintenance process for all Celerion processes and standards.\nEnsure processes and standards are compliant with regulatory requirements, corporate governances and the Quality Management System.\nDevelop, coordinate and facilitate training programs for appropriate processes and standards.\n"},{"text":"Requirements:","content":"\nBachelor's degree in Life Sciences or related degree preferred\nExcellent oral and written communication skills\nHigh proficiency in MS Office applications and Adobe Acrobat\nExcellent organization skills\nStrong facilitation, presentation and training skills\nSelf-motivated and able to perform with minimal supervision\n"}],"salaryRange":{"min":22,"max":23,"currency":"USD","interval":"per-hour-wage"},"text":"Standard Operating Procedure Designer - Lincoln, Nebraska","country":"US","workplaceType":"hybrid","opening":"Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
","openingPlain":"Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. \n","descriptionBody":"Celerion is currently seeking a full-time Standard Operating Procedure Designer for our Lincoln, Nebraska location. After 6-8 weeks of on-site training, you will have the ability to work primarily from home, if desired. You will work with your team in person and on-site every other week.
\n
\nIn this position, you will define, develop, implement and maintain Celerion standard processes that adhere to company governance and global regulatory requirements.
","descriptionBodyPlain":"Celerion is currently seeking a full-time Standard Operating Procedure Designer for our Lincoln, Nebraska location. After 6-8 weeks of on-site training, you will have the ability to work primarily from home, if desired. You will work with your team in person and on-site every other week.\n \nIn this position, you will define, develop, implement and maintain Celerion standard processes that adhere to company governance and global regulatory requirements.\n","hostedUrl":"https://jobs.lever.co/celerion/352890af-0c39-4f46-ad21-fc28f763a4a4","applyUrl":"https://jobs.lever.co/celerion/352890af-0c39-4f46-ad21-fc28f763a4a4/apply"},{"additionalPlain":"Celerion Values: Integrity Trust Teamwork Respect\n \nAre you ready to join our team?\n \nCelerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.\n \nNote: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as \"Not Junk\" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.\n \n","additional":"Celerion Values: Integrity Trust Teamwork Respect
\n
\nAre you ready to join our team?
\n
\nCelerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.
\n
\n\n
Note: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as \"Not Junk\" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.
\n
\n
Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
Spoken Spanish-English bilingual fluency is required in our Call Center. In this role, you will answer inbound calls from members of the public interested in participating in our Phase 1 clinical drug trials. You will screen callers for study eligibility, and then collect and enter personal data for those eligible to participate. You will also make outbound calls to schedule appointments, as needed.
\n
\nThis is a Benefitted Full-Time role which works 40 hours per week. The Call Center operates Monday-Saturday.
","id":"3d76728f-76bd-4c3e-8f89-513d67d1ddc4","lists":[{"text":"Requirements:","content":"\nHigh school diploma or GED\nMinimum 1 year of prior call center experience is required\nBilingual Spanish-English fluency is required\nPrior data entry experience is required\nMust be 18 years of age\nMust demonstrate excellent communication and customer service skills\n"},{"text":"Please Note:","content":"\nCandidates must have the ability to work a flexible schedule Monday-Saturday.\nInitial training occurs for 4-6 weeks during shifts scheduled 9AM-3PM.\nOnce training concludes, the regular work schedule is 40 hours per week\nTraining is onsite at our Screening Center in Tempe, AZ. \nWork may shift to home-based (within in the Phoenix, AZ metro area) after 90 days of good performance post-training. \n"}],"salaryRange":{"min":17.5,"max":17.5,"currency":"USD","interval":"per-hour-wage"},"text":"Study Participant Call Center Representative - Spanish Bilingual","country":"US","workplaceType":"hybrid","opening":"Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
","openingPlain":"Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. \n","descriptionBody":"Spoken Spanish-English bilingual fluency is required in our Call Center. In this role, you will answer inbound calls from members of the public interested in participating in our Phase 1 clinical drug trials. You will screen callers for study eligibility, and then collect and enter personal data for those eligible to participate. You will also make outbound calls to schedule appointments, as needed.
\n
\nThis is a Benefitted Full-Time role which works 40 hours per week. The Call Center operates Monday-Saturday.
","descriptionBodyPlain":"Spoken Spanish-English bilingual fluency is required in our Call Center. In this role, you will answer inbound calls from members of the public interested in participating in our Phase 1 clinical drug trials. You will screen callers for study eligibility, and then collect and enter personal data for those eligible to participate. You will also make outbound calls to schedule appointments, as needed.\n \nThis is a Benefitted Full-Time role which works 40 hours per week. The Call Center operates Monday-Saturday.\n","hostedUrl":"https://jobs.lever.co/celerion/3d76728f-76bd-4c3e-8f89-513d67d1ddc4","applyUrl":"https://jobs.lever.co/celerion/3d76728f-76bd-4c3e-8f89-513d67d1ddc4/apply"},{"additionalPlain":"Celerion Values: Integrity Trust Teamwork Respect\n \nCelerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.\n \nNote: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as \"Not Junk\" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.\n \n","additional":"Celerion Values: Integrity Trust Teamwork Respect
\n
\nCelerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.
\n
\n\n
Note: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as \"Not Junk\" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.
\n
\n
Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
Celerion has a 2nd shift Part-Time/ Variable opening for an Analyst – HPLC/LCMS in our Bioanalytical Division in Lincoln, NE. This position provides an hourly pay rate plus shift differential. This is a great opportunity for someone looking for evening work (4pm-12:30am) at least three nights per week.
\n
\nDo you have an interest in, or basic knowledge of, HPLC or LC/MS/MS techniques? If so, this could be the position for you! In this role, you will be responsible for performing analytical analysis of samples using chromatography and mass spectrometry in our nicotine-free laboratory environment.
\n
\nResponsibilities:
\nHired candidate will be trained to set up, operate, evaluate, monitor, troubleshoot system issues, instrument batches, and perform routine maintenance to the level of training on HPLC, and LC-MS/MS systems
\nResponsible for completing the minimum assigned daily lab duties of 4 batches
\nTake inventory of systems and equipment, active in column organization, prepare mobile phase and solutions
\nDocument clearly and accurately, and create, edit, and troubleshoot run sheets
\nProficient with all required quantification software programs
","id":"8de47fa1-5121-457b-a521-5e9ca75f14b3","lists":[{"text":"Qualifications:","content":"\nExperience in Mass spectrometry is preferred but is not required\nPrevious coursework in chemistry or a related field, with a degree preferred\nStrong mechanical inclination is a plus\nWe are seeking candidates with working knowledge of GLP’s.\nBasic knowledge of computers is also required\nBona Fide Occupational Qualification: This position requires candidates to be a non-nicotine/ tobacco user. This role is responsible for preparing solutions that cannot be contaminated with nicotine. This position is in continuous contact with the main glassware storage area which cannot be contaminated with nicotine. Nicotine is a volatile compound and a nicotine user simply being in the same room as the glassware can raise the nicotine levels in that glassware above our limit of detection and cause contamination issues in regards to our studies\n\n
\nShift:
\n\nMonday-Friday 4PM - 12:30AM - at least 20 hours per week, this position offers base plus shift differential\nOccasional weekend availability as needed\n\n
"}],"text":"Technician – HPLC/LCMS - 2nd shift (part-time)","country":"US","workplaceType":"onsite","opening":"Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
","openingPlain":"Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. \n","descriptionBody":"Celerion has a 2nd shift Part-Time/ Variable opening for an Analyst – HPLC/LCMS in our Bioanalytical Division in Lincoln, NE. This position provides an hourly pay rate plus shift differential. This is a great opportunity for someone looking for evening work (4pm-12:30am) at least three nights per week.
\n
\nDo you have an interest in, or basic knowledge of, HPLC or LC/MS/MS techniques? If so, this could be the position for you! In this role, you will be responsible for performing analytical analysis of samples using chromatography and mass spectrometry in our nicotine-free laboratory environment.
\n
\nResponsibilities:
\nHired candidate will be trained to set up, operate, evaluate, monitor, troubleshoot system issues, instrument batches, and perform routine maintenance to the level of training on HPLC, and LC-MS/MS systems
\nResponsible for completing the minimum assigned daily lab duties of 4 batches
\nTake inventory of systems and equipment, active in column organization, prepare mobile phase and solutions
\nDocument clearly and accurately, and create, edit, and troubleshoot run sheets
\nProficient with all required quantification software programs
","descriptionBodyPlain":"Celerion has a 2nd shift Part-Time/ Variable opening for an Analyst – HPLC/LCMS in our Bioanalytical Division in Lincoln, NE. This position provides an hourly pay rate plus shift differential. This is a great opportunity for someone looking for evening work (4pm-12:30am) at least three nights per week.\n \nDo you have an interest in, or basic knowledge of, HPLC or LC/MS/MS techniques? If so, this could be the position for you! In this role, you will be responsible for performing analytical analysis of samples using chromatography and mass spectrometry in our nicotine-free laboratory environment.\n \nResponsibilities:\nHired candidate will be trained to set up, operate, evaluate, monitor, troubleshoot system issues, instrument batches, and perform routine maintenance to the level of training on HPLC, and LC-MS/MS systems\nResponsible for completing the minimum assigned daily lab duties of 4 batches\nTake inventory of systems and equipment, active in column organization, prepare mobile phase and solutions\nDocument clearly and accurately, and create, edit, and troubleshoot run sheets\nProficient with all required quantification software programs\n","hostedUrl":"https://jobs.lever.co/celerion/8de47fa1-5121-457b-a521-5e9ca75f14b3","applyUrl":"https://jobs.lever.co/celerion/8de47fa1-5121-457b-a521-5e9ca75f14b3/apply"},{"additionalPlain":"Celerion Values: Integrity Trust Teamwork Respect\n \nAre you ready to join our team?\n \nCelerion is an Equal Opportunity Employer.\n","additional":"Celerion Values: Integrity Trust Teamwork Respect
\n
\nAre you ready to join our team?
\n
\nCelerion is an Equal Opportunity Employer.
","categories":{"commitment":"Full-Time","department":"Job Posting Categories","location":"Remote - UK","team":"Data Management and Biometrics","allLocations":["Remote - UK"]},"createdAt":1786529430947,"descriptionPlain":"TMF Representative\n \nJoin a team that's going places! Every member of Celerion is involved in making a distinctive contribution to the health and well-being of people around the world. That's the sense of purpose shared by our employees. We are a performance-driven drug research company, operating in robust and growing markets. We have an exciting future and offer a competitive salary in a strong developmental environment.\n \nCelerion, a leader in the clinical research industry, currently has an opportunity for a TMF Representative to join our team. This is a remote, home-based position within the UK. Applicants must have full and permanent right to work in the UK, Celerion does not currently offer Sponsorships.\n \nIn this position, you will be responsible for the preparation and the completeness of the Trial Master Files (TMF) for internal and external studies where Celerion has been contracted for the TMF services to meet Sponsor negotiated specifications. You will be responsible for maintenance of the Trial Master File, creating a file structure and indexing contents. You will also communicate with client Sponsors, Project Managers, monitors, sites and other study contacts to ensure compliance to protocol, and regulatory/local requirements.\n","description":"TMF Representative
\n
\nJoin a team that's going places! Every member of Celerion is involved in making a distinctive contribution to the health and well-being of people around the world. That's the sense of purpose shared by our employees. We are a performance-driven drug research company, operating in robust and growing markets. We have an exciting future and offer a competitive salary in a strong developmental environment.
\n
\nCelerion, a leader in the clinical research industry, currently has an opportunity for a TMF Representative to join our team. This is a remote, home-based position within the UK. Applicants must have full and permanent right to work in the UK, Celerion does not currently offer Sponsorships.
\n
\nIn this position, you will be responsible for the preparation and the completeness of the Trial Master Files (TMF) for internal and external studies where Celerion has been contracted for the TMF services to meet Sponsor negotiated specifications. You will be responsible for maintenance of the Trial Master File, creating a file structure and indexing contents. You will also communicate with client Sponsors, Project Managers, monitors, sites and other study contacts to ensure compliance to protocol, and regulatory/local requirements.
","id":"c2fb7a29-083f-4437-8c44-71a6a6518ac8","lists":[{"text":"Requirements ","content":"\nBachelor's degree in related field such as science or other biomedical discipline\nExperience in clinical research and/or Trial Master Files preferred\nMinimum 1 year document management experience.\nExcellent interpersonal and oral/ written communication skills.\nHighly organized and collaborative.\nProficient computer skills, i.e., MS Word, Excel, PowerPoint.\nAbility to manage multiple priorities\n"}],"text":"Trial Master File Representative (Remote - UK)","country":"GB","workplaceType":"remote","opening":"","openingPlain":"","descriptionBody":"TMF Representative
\n
\nJoin a team that's going places! Every member of Celerion is involved in making a distinctive contribution to the health and well-being of people around the world. That's the sense of purpose shared by our employees. We are a performance-driven drug research company, operating in robust and growing markets. We have an exciting future and offer a competitive salary in a strong developmental environment.
\n
\nCelerion, a leader in the clinical research industry, currently has an opportunity for a TMF Representative to join our team. This is a remote, home-based position within the UK. Applicants must have full and permanent right to work in the UK, Celerion does not currently offer Sponsorships.
\n
\nIn this position, you will be responsible for the preparation and the completeness of the Trial Master Files (TMF) for internal and external studies where Celerion has been contracted for the TMF services to meet Sponsor negotiated specifications. You will be responsible for maintenance of the Trial Master File, creating a file structure and indexing contents. You will also communicate with client Sponsors, Project Managers, monitors, sites and other study contacts to ensure compliance to protocol, and regulatory/local requirements.
","descriptionBodyPlain":"TMF Representative\n \nJoin a team that's going places! Every member of Celerion is involved in making a distinctive contribution to the health and well-being of people around the world. That's the sense of purpose shared by our employees. We are a performance-driven drug research company, operating in robust and growing markets. We have an exciting future and offer a competitive salary in a strong developmental environment.\n \nCelerion, a leader in the clinical research industry, currently has an opportunity for a TMF Representative to join our team. This is a remote, home-based position within the UK. Applicants must have full and permanent right to work in the UK, Celerion does not currently offer Sponsorships.\n \nIn this position, you will be responsible for the preparation and the completeness of the Trial Master Files (TMF) for internal and external studies where Celerion has been contracted for the TMF services to meet Sponsor negotiated specifications. You will be responsible for maintenance of the Trial Master File, creating a file structure and indexing contents. You will also communicate with client Sponsors, Project Managers, monitors, sites and other study contacts to ensure compliance to protocol, and regulatory/local requirements.\n","hostedUrl":"https://jobs.lever.co/celerion/c2fb7a29-083f-4437-8c44-71a6a6518ac8","applyUrl":"https://jobs.lever.co/celerion/c2fb7a29-083f-4437-8c44-71a6a6518ac8/apply"},{"additionalPlain":"Celerion Values: Integrity Trust Teamwork Respect\n \nCelerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.\n \nNote: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as \"Not Junk\" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.\n \n","additional":"Celerion Values: Integrity Trust Teamwork Respect
\n
\nCelerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.
\n
\n\n
Note: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as \"Not Junk\" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.
\n
\n
Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
Are you looking for an opportunity to support a business creating life-saving treatments? If so, we can't wait to meet you!
\n
\nWe are looking for a performance-oriented, innovative and self-motivated team player to join our Clinical Data Sciences team as a full-time Veeva Clinical Database Programmer. You will be responsible for the administration of EDC database, including evaluation, analysis, design and/ or recommendations to achieve goals and excellent results in a fast-paced, ever-changing environment.
\n
\nThis is a full-time, remote opportunity, but you may travel for training and key meetings.
\n
\nAs a Veeva Clinical Database Programmer, you will build and administer EDC trials for client-contracted projects, including protocol/requirements evaluation, electronic case report form (eCRF) design and build with corresponding edits. This role will have technical interaction with vendors that are supporting the applications and troubleshoot/ escalate problems on systems to appropriate partners. This role will provide expert guidance to the design, development, validation, implementation and maintenance of study set-up. Additionally, this role will manage the deployment of EDC trials and set up interface connections between EDC and other systems.
\n
","id":"e1d04ca4-897f-4c62-acf0-47126d4aaeac","lists":[{"text":"In this role you will:","content":"\nServe as a subject matter expert in Veeva Clinical Data Management Suite (CDMS), including Veeva Electronic Data Capture (EDC) and Veeva Clinical Database (CDB)\nPerform all activities related to eCRF design and EDC build programming for assigned projects\nPerform EDC edit check programming for assigned projects based on edit check specifications for both simple and complex edit checks\nCreate test data to verify both screen design and edit check programming prior to deploying to User Acceptance Testing (UAT)\nSet up test environments and coordinate project team members for execution of test scripts\nProgram and configure listings and reports using clinical reporting tools such as Veeva Clinical Database (CDB)\nEnsure secure and high-integrity database imports from vendor transfers using Celerion data transfer standards\nAssist with the validation of upgrades to hardware/ software including validation documentation development, review and execution.\nMaintain global clinical trial database standards (CDISC)\n"},{"text":"Requirements:","content":"\nBachelor’s degree in a related field preferred\n3 years of clinical data management experience\nAbility to program using SQL required\nExperience with Veeva EDC and Veeva CDB \nProficient computer skills with understanding of clinical systems and data administration\nMust be organized, an effective written and oral communicator\nMust have the ability to multi-task, within a fast-paced environment, and build strong relationships \n\n
\n#LI-Remote
"}],"text":"Veeva Clinical Database Programmer","country":"US","workplaceType":"remote","opening":"Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
","openingPlain":"Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. \n","descriptionBody":"Are you looking for an opportunity to support a business creating life-saving treatments? If so, we can't wait to meet you!
\n
\nWe are looking for a performance-oriented, innovative and self-motivated team player to join our Clinical Data Sciences team as a full-time Veeva Clinical Database Programmer. You will be responsible for the administration of EDC database, including evaluation, analysis, design and/ or recommendations to achieve goals and excellent results in a fast-paced, ever-changing environment.
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\nThis is a full-time, remote opportunity, but you may travel for training and key meetings.
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\nAs a Veeva Clinical Database Programmer, you will build and administer EDC trials for client-contracted projects, including protocol/requirements evaluation, electronic case report form (eCRF) design and build with corresponding edits. This role will have technical interaction with vendors that are supporting the applications and troubleshoot/ escalate problems on systems to appropriate partners. This role will provide expert guidance to the design, development, validation, implementation and maintenance of study set-up. Additionally, this role will manage the deployment of EDC trials and set up interface connections between EDC and other systems.
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","descriptionBodyPlain":"Are you looking for an opportunity to support a business creating life-saving treatments? If so, we can't wait to meet you!\n \nWe are looking for a performance-oriented, innovative and self-motivated team player to join our Clinical Data Sciences team as a full-time Veeva Clinical Database Programmer. You will be responsible for the administration of EDC database, including evaluation, analysis, design and/ or recommendations to achieve goals and excellent results in a fast-paced, ever-changing environment.\n \nThis is a full-time, remote opportunity, but you may travel for training and key meetings.\n \nAs a Veeva Clinical Database Programmer, you will build and administer EDC trials for client-contracted projects, including protocol/requirements evaluation, electronic case report form (eCRF) design and build with corresponding edits. This role will have technical interaction with vendors that are supporting the applications and troubleshoot/ escalate problems on systems to appropriate partners. This role will provide expert guidance to the design, development, validation, implementation and maintenance of study set-up. Additionally, this role will manage the deployment of EDC trials and set up interface connections between EDC and other systems.\n \n","hostedUrl":"https://jobs.lever.co/celerion/e1d04ca4-897f-4c62-acf0-47126d4aaeac","applyUrl":"https://jobs.lever.co/celerion/e1d04ca4-897f-4c62-acf0-47126d4aaeac/apply"}]