Physical Requirements & Work Environment
\nThis role is performed on-site at a clinical or office facility and requires prolonged periods of sitting, standing, or walking throughout the work environment
\nRequires the ability to communicate clearly in verbal and written forms and to read and interpret detailed materials
\nMust be able to navigate a clinical facility, including areas with limited space, and transport supplies or work materials as needed
\nMay be required to wear personal protective equipment (PPE) in accordance with facility protocols
\nTravel between company sites, meetings, or partner locations may be required
\nReasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the role
\n\n
Why Join Profound Research?
\nMeaningful Impact: Every role at Profound contributes to advancing medical knowledge and expanding therapeutic options for patients – the work we do here matters
\nProfessional Growth: We invest in our people through comprehensive training, certification support, and ongoing education to help you grow in your role and your career
\nLeadership & Advancement: Profound is a place where initiative is recognized. We actively support internal growth and create pathways for people to take on greater responsibility over time
\nCollaborative Culture: You’ll work alongside a team of dedicated professionals who are passionate about clinical research and committed to doing it well
\nFull Benefits Package: Competitive compensation, health insurance, PTO, retirement plan, and professional development support
\nDiverse Clinical Exposure: Work across multiple therapeutic areas and study phases, building a breadth of experience that’s rare in a single organization (for Clinical / Patient-Facing roles)
\nStart Your Career in Clinical Research
\nIf you’re curious about how new treatments reach patients, detail-oriented by nature, and energized by work that genuinely matters – this is where that career begins.
\n\n
As an Assistant Clinical Research Coordinator at Profound Research, you’ll work alongside experienced clinical research staff at one of our sites, supporting the day-to-day execution of clinical trials that give patients access to therapies they couldn’t otherwise reach. You’ll learn by doing – gaining hands-on experience in study coordination, patient interaction, data collection, and clinical procedures – with a clear path to grow into greater ownership and responsibility over time.
\n\n
This isn’t a behind-the-desk role. You’ll be present with patients, part of a team, and contributing to research that has real-world impact from day one.
\n\n
What You’ll Do
\n\n
Support the coordination of active clinical trials, including patient visits, scheduling, and study-related procedures
\nAssist with data collection and documentation, learning to apply the rigorous standards that clinical research demands
\nPerform and develop competency in clinical procedures including vital signs, EKGs, phlebotomy, and specimen processing
\nInteract directly with study participants – greeting them, explaining visit steps, and ensuring they feel supported throughout the process
\nWork closely with Clinical Research Coordinators and site leadership, asking questions, seeking feedback, and building your clinical knowledge base
\nContribute to a compliant, audit-ready site by following established protocols, SOPs, and Good Documentation Practices
\n\n
What We’re Looking For
\nYou don’t need to have done this exact job before. You need to be the kind of person who takes ownership of their work, communicates clearly, pays close attention to detail, and genuinely cares about the patient experience. The rest we’ll help you build.
\n\n
High school diploma or technical degree with 3+ years of relevant experience in life sciences, OR Associate’s degree with 1+ year of relevant experience, OR Bachelor’s degree with relevant coursework or experience in a clinical or life sciences setting
\nFamiliarity with medical terminology and basic clinical procedures is a plus
\nComfortable working in a fast-paced, team-based environment
\nProficient with standard computer tools; able to learn new systems quickly
\nICH-GCP and IATA certification required within a defined timeframe upon hire (we’ll support you through it)
\nStart Your Career in Clinical Research
\nIf you’re curious about how new treatments reach patients, detail-oriented by nature, and energized by work that genuinely matters – this is where that career begins.
\n\n
As an Assistant Clinical Research Coordinator at Profound Research, you’ll work alongside experienced clinical research staff at one of our sites, supporting the day-to-day execution of clinical trials that give patients access to therapies they couldn’t otherwise reach. You’ll learn by doing – gaining hands-on experience in study coordination, patient interaction, data collection, and clinical procedures – with a clear path to grow into greater ownership and responsibility over time.
\n\n
This isn’t a behind-the-desk role. You’ll be present with patients, part of a team, and contributing to research that has real-world impact from day one.
\n\n
What You’ll Do
\n\n
Support the coordination of active clinical trials, including patient visits, scheduling, and study-related procedures
\nAssist with data collection and documentation, learning to apply the rigorous standards that clinical research demands
\nPerform and develop competency in clinical procedures including vital signs, EKGs, phlebotomy, and specimen processing
\nInteract directly with study participants – greeting them, explaining visit steps, and ensuring they feel supported throughout the process
\nWork closely with Clinical Research Coordinators and site leadership, asking questions, seeking feedback, and building your clinical knowledge base
\nContribute to a compliant, audit-ready site by following established protocols, SOPs, and Good Documentation Practices
\n\n
What We’re Looking For
\nYou don’t need to have done this exact job before. You need to be the kind of person who takes ownership of their work, communicates clearly, pays close attention to detail, and genuinely cares about the patient experience. The rest we’ll help you build.
\n\n
High school diploma or technical degree with 3+ years of relevant experience in life sciences, OR Associate’s degree with 1+ year of relevant experience, OR Bachelor’s degree with relevant coursework or experience in a clinical or life sciences setting
\nFamiliarity with medical terminology and basic clinical procedures is a plus
\nComfortable working in a fast-paced, team-based environment
\nProficient with standard computer tools; able to learn new systems quickly
\nICH-GCP and IATA certification required within a defined timeframe upon hire (we’ll support you through it)
\nPhysical Requirements & Work Environment
\nThis role is performed on-site at a clinical or office facility and requires prolonged periods of sitting, standing, or walking throughout the work environment
\nRequires the ability to communicate clearly in verbal and written forms and to read and interpret detailed materials
\nMust be able to navigate a clinical facility, including areas with limited space, and transport supplies or work materials as needed
\nMay be required to wear personal protective equipment (PPE) in accordance with facility protocols
\nTravel between company sites, meetings, or partner locations may be required
\nReasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the role
\n\n
Why Join Profound Research?
\nMeaningful Impact: Every role at Profound contributes to advancing medical knowledge and expanding therapeutic options for patients – the work we do here matters
\nProfessional Growth: We invest in our people through comprehensive training, certification support, and ongoing education to help you grow in your role and your career
\nLeadership & Advancement: Profound is a place where initiative is recognized. We actively support internal growth and create pathways for people to take on greater responsibility over time
\nCollaborative Culture: You’ll work alongside a team of dedicated professionals who are passionate about clinical research and committed to doing it well
\nFull Benefits Package: Competitive compensation, health insurance, PTO, retirement plan, and professional development support
\nDiverse Clinical Exposure: Work across multiple therapeutic areas and study phases, building a breadth of experience that’s rare in a single organization (for Clinical / Patient-Facing roles)
\nOwn Your Studies. Grow Your Career.
\nIf you’re ready to step into real ownership of clinical trial coordination – managing your own studies, leading patient visits, and working with the independence that comes from having built a strong foundation – this role is the next step.
\n\n
As a Clinical Research Coordinator I at Profound Research, you’ll serve as the primary coordinator for assigned studies at one of our sites. You’ll manage study activities from start-up through closeout, lead interactions with study participants, maintain audit-ready documentation, and work directly with investigators, sponsors, and CROs. This isn’t a support role – you own your studies, and your work directly impacts patient safety, data integrity, and trial outcomes.
\n\n
What You’ll Do
\n\n
Serve as primary coordinator for assigned clinical trials, managing study activities from start-up through closeout
\nExecute full visit flow independently – participant visits, protocol procedures, data collection, and documentation
\nLead patient interactions with clarity and compassion, ensuring participants feel informed and supported throughout their study experience
\nMaintain accurate, timely, audit-ready documentation across source documents, CRFs, and EDC systems
\nTrack and report adverse events, deviations, and safety findings in accordance with protocol and regulatory requirements
\nCommunicate directly and professionally with investigators, sponsors, CROs, and internal teams
\nSupport site readiness for monitoring visits and audits
\n\n
What We’re Looking For
\nYou’ve got some experience in clinical research and you’re ready for more responsibility. You’re organized, detail-oriented, and comfortable working independently. You take ownership of your work and follow through without being reminded.
\n\n
Bachelor’s degree with 1+ year of relevant experience, OR Associate’s degree with 3+ years of relevant experience, OR High school diploma with 4+ years of relevant experience and at least 1 year of CRC experience
\nExperience performing clinical procedures including vital signs, EKGs, phlebotomy, and lab processing
\nComfortable working independently and managing competing priorities
\nStrong documentation skills and familiarity with EDC platforms and clinical trial management systems
\nOwn Your Studies. Grow Your Career.
\nIf you’re ready to step into real ownership of clinical trial coordination – managing your own studies, leading patient visits, and working with the independence that comes from having built a strong foundation – this role is the next step.
\n\n
As a Clinical Research Coordinator I at Profound Research, you’ll serve as the primary coordinator for assigned studies at one of our sites. You’ll manage study activities from start-up through closeout, lead interactions with study participants, maintain audit-ready documentation, and work directly with investigators, sponsors, and CROs. This isn’t a support role – you own your studies, and your work directly impacts patient safety, data integrity, and trial outcomes.
\n\n
What You’ll Do
\n\n
Serve as primary coordinator for assigned clinical trials, managing study activities from start-up through closeout
\nExecute full visit flow independently – participant visits, protocol procedures, data collection, and documentation
\nLead patient interactions with clarity and compassion, ensuring participants feel informed and supported throughout their study experience
\nMaintain accurate, timely, audit-ready documentation across source documents, CRFs, and EDC systems
\nTrack and report adverse events, deviations, and safety findings in accordance with protocol and regulatory requirements
\nCommunicate directly and professionally with investigators, sponsors, CROs, and internal teams
\nSupport site readiness for monitoring visits and audits
\n\n
What We’re Looking For
\nYou’ve got some experience in clinical research and you’re ready for more responsibility. You’re organized, detail-oriented, and comfortable working independently. You take ownership of your work and follow through without being reminded.
\n\n
Bachelor’s degree with 1+ year of relevant experience, OR Associate’s degree with 3+ years of relevant experience, OR High school diploma with 4+ years of relevant experience and at least 1 year of CRC experience
\nExperience performing clinical procedures including vital signs, EKGs, phlebotomy, and lab processing
\nComfortable working independently and managing competing priorities
\nStrong documentation skills and familiarity with EDC platforms and clinical trial management systems
\nPhysical Requirements & Work Environment
\nThis role is performed on-site at a clinical or office facility and requires prolonged periods of sitting, standing, or walking throughout the work environment
\nRequires the ability to communicate clearly in verbal and written forms and to read and interpret detailed materials
\nMust be able to navigate a clinical facility, including areas with limited space, and transport supplies or work materials as needed
\nMay be required to wear personal protective equipment (PPE) in accordance with facility protocols
\nTravel between company sites, meetings, or partner locations may be required
\nReasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the role
\n\n
Why Join Profound Research?
\nMeaningful Impact: Every role at Profound contributes to advancing medical knowledge and expanding therapeutic options for patients – the work we do here matters
\nProfessional Growth: We invest in our people through comprehensive training, certification support, and ongoing education to help you grow in your role and your career
\nLeadership & Advancement: Profound is a place where initiative is recognized. We actively support internal growth and create pathways for people to take on greater responsibility over time
\nCollaborative Culture: You’ll work alongside a team of dedicated professionals who are passionate about clinical research and committed to doing it well
\nFull Benefits Package: Competitive compensation, health insurance, PTO, retirement plan, and professional development support
\nDiverse Clinical Exposure: Work across multiple therapeutic areas and study phases, building a breadth of experience that’s rare in a single organization (for Clinical / Patient-Facing roles)
\nOwn Your Studies. Grow Your Career.
\nIf you’re ready to step into real ownership of clinical trial coordination – managing your own studies, leading patient visits, and working with the independence that comes from having built a strong foundation – this role is the next step.
\n\n
As a Clinical Research Coordinator I at Profound Research, you’ll serve as the primary coordinator for assigned studies at one of our sites. You’ll manage study activities from start-up through closeout, lead interactions with study participants, maintain audit-ready documentation, and work directly with investigators, sponsors, and CROs. This isn’t a support role – you own your studies, and your work directly impacts patient safety, data integrity, and trial outcomes.
\n\n
What You’ll Do
\n\n
Serve as primary coordinator for assigned clinical trials, managing study activities from start-up through closeout
\nExecute full visit flow independently – participant visits, protocol procedures, data collection, and documentation
\nLead patient interactions with clarity and compassion, ensuring participants feel informed and supported throughout their study experience
\nMaintain accurate, timely, audit-ready documentation across source documents, CRFs, and EDC systems
\nTrack and report adverse events, deviations, and safety findings in accordance with protocol and regulatory requirements
\nCommunicate directly and professionally with investigators, sponsors, CROs, and internal teams
\nSupport site readiness for monitoring visits and audits
\n\n
What We’re Looking For
\nYou’ve got some experience in clinical research and you’re ready for more responsibility. You’re organized, detail-oriented, and comfortable working independently. You take ownership of your work and follow through without being reminded.
\n\n
Bachelor’s degree with 1+ year of relevant experience, OR Associate’s degree with 3+ years of relevant experience, OR High school diploma with 4+ years of relevant experience and at least 1 year of CRC experience
\nExperience performing clinical procedures including vital signs, EKGs, phlebotomy, and lab processing
\nComfortable working independently and managing competing priorities
\nStrong documentation skills and familiarity with EDC platforms and clinical trial management systems
\nOwn Your Studies. Grow Your Career.
\nIf you’re ready to step into real ownership of clinical trial coordination – managing your own studies, leading patient visits, and working with the independence that comes from having built a strong foundation – this role is the next step.
\n\n
As a Clinical Research Coordinator I at Profound Research, you’ll serve as the primary coordinator for assigned studies at one of our sites. You’ll manage study activities from start-up through closeout, lead interactions with study participants, maintain audit-ready documentation, and work directly with investigators, sponsors, and CROs. This isn’t a support role – you own your studies, and your work directly impacts patient safety, data integrity, and trial outcomes.
\n\n
What You’ll Do
\n\n
Serve as primary coordinator for assigned clinical trials, managing study activities from start-up through closeout
\nExecute full visit flow independently – participant visits, protocol procedures, data collection, and documentation
\nLead patient interactions with clarity and compassion, ensuring participants feel informed and supported throughout their study experience
\nMaintain accurate, timely, audit-ready documentation across source documents, CRFs, and EDC systems
\nTrack and report adverse events, deviations, and safety findings in accordance with protocol and regulatory requirements
\nCommunicate directly and professionally with investigators, sponsors, CROs, and internal teams
\nSupport site readiness for monitoring visits and audits
\n\n
What We’re Looking For
\nYou’ve got some experience in clinical research and you’re ready for more responsibility. You’re organized, detail-oriented, and comfortable working independently. You take ownership of your work and follow through without being reminded.
\n\n
Bachelor’s degree with 1+ year of relevant experience, OR Associate’s degree with 3+ years of relevant experience, OR High school diploma with 4+ years of relevant experience and at least 1 year of CRC experience
\nExperience performing clinical procedures including vital signs, EKGs, phlebotomy, and lab processing
\nComfortable working independently and managing competing priorities
\nStrong documentation skills and familiarity with EDC platforms and clinical trial management systems
\nPhysical Requirements & Work Environment
\nThis role is performed on-site at a clinical or office facility and requires prolonged periods of sitting, standing, or walking throughout the work environment
\nRequires the ability to communicate clearly in verbal and written forms and to read and interpret detailed materials
\nMust be able to navigate a clinical facility, including areas with limited space, and transport supplies or work materials as needed
\nMay be required to wear personal protective equipment (PPE) in accordance with facility protocols
\nTravel between company sites, meetings, or partner locations may be required
\nReasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the role
\n\n
Why Join Profound Research?
\nMeaningful Impact: Every role at Profound contributes to advancing medical knowledge and expanding therapeutic options for patients – the work we do here matters
\nProfessional Growth: We invest in our people through comprehensive training, certification support, and ongoing education to help you grow in your role and your career
\nLeadership & Advancement: Profound is a place where initiative is recognized. We actively support internal growth and create pathways for people to take on greater responsibility over time
\nCollaborative Culture: You’ll work alongside a team of dedicated professionals who are passionate about clinical research and committed to doing it well
\nFull Benefits Package: Competitive compensation, health insurance, PTO, retirement plan, and professional development support
\nDiverse Clinical Exposure: Work across multiple therapeutic areas and study phases, building a breadth of experience that’s rare in a single organization (for Clinical / Patient-Facing roles)
\nOwn Your Studies. Grow Your Career.
\nIf you’re ready to step into real ownership of clinical trial coordination – managing your own studies, leading patient visits, and working with the independence that comes from having built a strong foundation – this role is the next step.
\n\n
As a Clinical Research Coordinator I at Profound Research, you’ll serve as the primary coordinator for assigned studies at one of our sites. You’ll manage study activities from start-up through closeout, lead interactions with study participants, maintain audit-ready documentation, and work directly with investigators, sponsors, and CROs. This isn’t a support role – you own your studies, and your work directly impacts patient safety, data integrity, and trial outcomes.
\n\n
What You’ll Do
\n\n
Serve as primary coordinator for assigned clinical trials, managing study activities from start-up through closeout
\nExecute full visit flow independently – participant visits, protocol procedures, data collection, and documentation
\nLead patient interactions with clarity and compassion, ensuring participants feel informed and supported throughout their study experience
\nMaintain accurate, timely, audit-ready documentation across source documents, CRFs, and EDC systems
\nTrack and report adverse events, deviations, and safety findings in accordance with protocol and regulatory requirements
\nCommunicate directly and professionally with investigators, sponsors, CROs, and internal teams
\nSupport site readiness for monitoring visits and audits
\n\n
What We’re Looking For
\nYou’ve got some experience in clinical research and you’re ready for more responsibility. You’re organized, detail-oriented, and comfortable working independently. You take ownership of your work and follow through without being reminded.
\n\n
Bachelor’s degree with 1+ year of relevant experience, OR Associate’s degree with 3+ years of relevant experience, OR High school diploma with 4+ years of relevant experience and at least 1 year of CRC experience
\nExperience performing clinical procedures including vital signs, EKGs, phlebotomy, and lab processing
\nComfortable working independently and managing competing priorities
\nStrong documentation skills and familiarity with EDC platforms and clinical trial management systems
\nOwn Your Studies. Grow Your Career.
\nIf you’re ready to step into real ownership of clinical trial coordination – managing your own studies, leading patient visits, and working with the independence that comes from having built a strong foundation – this role is the next step.
\n\n
As a Clinical Research Coordinator I at Profound Research, you’ll serve as the primary coordinator for assigned studies at one of our sites. You’ll manage study activities from start-up through closeout, lead interactions with study participants, maintain audit-ready documentation, and work directly with investigators, sponsors, and CROs. This isn’t a support role – you own your studies, and your work directly impacts patient safety, data integrity, and trial outcomes.
\n\n
What You’ll Do
\n\n
Serve as primary coordinator for assigned clinical trials, managing study activities from start-up through closeout
\nExecute full visit flow independently – participant visits, protocol procedures, data collection, and documentation
\nLead patient interactions with clarity and compassion, ensuring participants feel informed and supported throughout their study experience
\nMaintain accurate, timely, audit-ready documentation across source documents, CRFs, and EDC systems
\nTrack and report adverse events, deviations, and safety findings in accordance with protocol and regulatory requirements
\nCommunicate directly and professionally with investigators, sponsors, CROs, and internal teams
\nSupport site readiness for monitoring visits and audits
\n\n
What We’re Looking For
\nYou’ve got some experience in clinical research and you’re ready for more responsibility. You’re organized, detail-oriented, and comfortable working independently. You take ownership of your work and follow through without being reminded.
\n\n
Bachelor’s degree with 1+ year of relevant experience, OR Associate’s degree with 3+ years of relevant experience, OR High school diploma with 4+ years of relevant experience and at least 1 year of CRC experience
\nExperience performing clinical procedures including vital signs, EKGs, phlebotomy, and lab processing
\nComfortable working independently and managing competing priorities
\nStrong documentation skills and familiarity with EDC platforms and clinical trial management systems
\nPhysical Requirements & Work Environment
\nThis role is performed on-site at a clinical or office facility and requires prolonged periods of sitting, standing, or walking throughout the work environment
\nRequires the ability to communicate clearly in verbal and written forms and to read and interpret detailed materials
\nMust be able to navigate a clinical facility, including areas with limited space, and transport supplies or work materials as needed
\nMay be required to wear personal protective equipment (PPE) in accordance with facility protocols
\nTravel between company sites, meetings, or partner locations may be required
\nReasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the role
\n\n
Why Join Profound Research?
\nMeaningful Impact: Every role at Profound contributes to advancing medical knowledge and expanding therapeutic options for patients – the work we do here matters
\nProfessional Growth: We invest in our people through comprehensive training, certification support, and ongoing education to help you grow in your role and your career
\nLeadership & Advancement: Profound is a place where initiative is recognized. We actively support internal growth and create pathways for people to take on greater responsibility over time
\nCollaborative Culture: You’ll work alongside a team of dedicated professionals who are passionate about clinical research and committed to doing it well
\nFull Benefits Package: Competitive compensation, health insurance, PTO, retirement plan, and professional development support
\nDiverse Clinical Exposure: Work across multiple therapeutic areas and study phases, building a breadth of experience that’s rare in a single organization (for Clinical / Patient-Facing roles)
\nOwn Your Studies. Grow Your Career.
\nIf you’re ready to step into real ownership of clinical trial coordination – managing your own studies, leading patient visits, and working with the independence that comes from having built a strong foundation – this role is the next step.
\n\n
As a Clinical Research Coordinator I at Profound Research, you’ll serve as the primary coordinator for assigned studies at one of our sites. You’ll manage study activities from start-up through closeout, lead interactions with study participants, maintain audit-ready documentation, and work directly with investigators, sponsors, and CROs. This isn’t a support role – you own your studies, and your work directly impacts patient safety, data integrity, and trial outcomes.
\n\n
What You’ll Do
\n\n
Serve as primary coordinator for assigned clinical trials, managing study activities from start-up through closeout
\nExecute full visit flow independently – participant visits, protocol procedures, data collection, and documentation
\nLead patient interactions with clarity and compassion, ensuring participants feel informed and supported throughout their study experience
\nMaintain accurate, timely, audit-ready documentation across source documents, CRFs, and EDC systems
\nTrack and report adverse events, deviations, and safety findings in accordance with protocol and regulatory requirements
\nCommunicate directly and professionally with investigators, sponsors, CROs, and internal teams
\nSupport site readiness for monitoring visits and audits
\n\n
What We’re Looking For
\nYou’ve got some experience in clinical research and you’re ready for more responsibility. You’re organized, detail-oriented, and comfortable working independently. You take ownership of your work and follow through without being reminded.
\n\n
Bachelor’s degree with 1+ year of relevant experience, OR Associate’s degree with 3+ years of relevant experience, OR High school diploma with 4+ years of relevant experience and at least 1 year of CRC experience
\nExperience performing clinical procedures including vital signs, EKGs, phlebotomy, and lab processing
\nComfortable working independently and managing competing priorities
\nStrong documentation skills and familiarity with EDC platforms and clinical trial management systems
\nOwn Your Studies. Grow Your Career.
\nIf you’re ready to step into real ownership of clinical trial coordination – managing your own studies, leading patient visits, and working with the independence that comes from having built a strong foundation – this role is the next step.
\n\n
As a Clinical Research Coordinator I at Profound Research, you’ll serve as the primary coordinator for assigned studies at one of our sites. You’ll manage study activities from start-up through closeout, lead interactions with study participants, maintain audit-ready documentation, and work directly with investigators, sponsors, and CROs. This isn’t a support role – you own your studies, and your work directly impacts patient safety, data integrity, and trial outcomes.
\n\n
What You’ll Do
\n\n
Serve as primary coordinator for assigned clinical trials, managing study activities from start-up through closeout
\nExecute full visit flow independently – participant visits, protocol procedures, data collection, and documentation
\nLead patient interactions with clarity and compassion, ensuring participants feel informed and supported throughout their study experience
\nMaintain accurate, timely, audit-ready documentation across source documents, CRFs, and EDC systems
\nTrack and report adverse events, deviations, and safety findings in accordance with protocol and regulatory requirements
\nCommunicate directly and professionally with investigators, sponsors, CROs, and internal teams
\nSupport site readiness for monitoring visits and audits
\n\n
What We’re Looking For
\nYou’ve got some experience in clinical research and you’re ready for more responsibility. You’re organized, detail-oriented, and comfortable working independently. You take ownership of your work and follow through without being reminded.
\n\n
Bachelor’s degree with 1+ year of relevant experience, OR Associate’s degree with 3+ years of relevant experience, OR High school diploma with 4+ years of relevant experience and at least 1 year of CRC experience
\nExperience performing clinical procedures including vital signs, EKGs, phlebotomy, and lab processing
\nComfortable working independently and managing competing priorities
\nStrong documentation skills and familiarity with EDC platforms and clinical trial management systems
\nPhysical Requirements & Work Environment
\nThis role is performed on-site at a clinical or office facility and requires prolonged periods of sitting, standing, or walking throughout the work environment
\nRequires the ability to communicate clearly in verbal and written forms and to read and interpret detailed materials
\nMust be able to navigate a clinical facility, including areas with limited space, and transport supplies or work materials as needed
\nMay be required to wear personal protective equipment (PPE) in accordance with facility protocols
\nTravel between company sites, meetings, or partner locations may be required
\nReasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the role
\n\n
Why Join Profound Research?
\nMeaningful Impact: Every role at Profound contributes to advancing medical knowledge and expanding therapeutic options for patients – the work we do here matters
\nProfessional Growth: We invest in our people through comprehensive training, certification support, and ongoing education to help you grow in your role and your career
\nLeadership & Advancement: Profound is a place where initiative is recognized. We actively support internal growth and create pathways for people to take on greater responsibility over time
\nCollaborative Culture: You’ll work alongside a team of dedicated professionals who are passionate about clinical research and committed to doing it well
\nFull Benefits Package: Competitive compensation, health insurance, PTO, retirement plan, and professional development support
\nDiverse Clinical Exposure: Work across multiple therapeutic areas and study phases, building a breadth of experience that’s rare in a single organization (for Clinical / Patient-Facing roles)
\nOwn Your Studies. Grow Your Career.
\nIf you’re ready to step into real ownership of clinical trial coordination – managing your own studies, leading patient visits, and working with the independence that comes from having built a strong foundation – this role is the next step.
\n\n
As a Clinical Research Coordinator I at Profound Research, you’ll serve as the primary coordinator for assigned studies at one of our sites. You’ll manage study activities from start-up through closeout, lead interactions with study participants, maintain audit-ready documentation, and work directly with investigators, sponsors, and CROs. This isn’t a support role – you own your studies, and your work directly impacts patient safety, data integrity, and trial outcomes.
\n\n
What You’ll Do
\n\n
Serve as primary coordinator for assigned clinical trials, managing study activities from start-up through closeout
\nExecute full visit flow independently – participant visits, protocol procedures, data collection, and documentation
\nLead patient interactions with clarity and compassion, ensuring participants feel informed and supported throughout their study experience
\nMaintain accurate, timely, audit-ready documentation across source documents, CRFs, and EDC systems
\nTrack and report adverse events, deviations, and safety findings in accordance with protocol and regulatory requirements
\nCommunicate directly and professionally with investigators, sponsors, CROs, and internal teams
\nSupport site readiness for monitoring visits and audits
\n\n
What We’re Looking For
\nYou’ve got some experience in clinical research and you’re ready for more responsibility. You’re organized, detail-oriented, and comfortable working independently. You take ownership of your work and follow through without being reminded.
\n\n
Bachelor’s degree with 1+ year of relevant experience, OR Associate’s degree with 3+ years of relevant experience, OR High school diploma with 4+ years of relevant experience and at least 1 year of CRC experience
\nExperience performing clinical procedures including vital signs, EKGs, phlebotomy, and lab processing
\nComfortable working independently and managing competing priorities
\nStrong documentation skills and familiarity with EDC platforms and clinical trial management systems
\nOwn Your Studies. Grow Your Career.
\nIf you’re ready to step into real ownership of clinical trial coordination – managing your own studies, leading patient visits, and working with the independence that comes from having built a strong foundation – this role is the next step.
\n\n
As a Clinical Research Coordinator I at Profound Research, you’ll serve as the primary coordinator for assigned studies at one of our sites. You’ll manage study activities from start-up through closeout, lead interactions with study participants, maintain audit-ready documentation, and work directly with investigators, sponsors, and CROs. This isn’t a support role – you own your studies, and your work directly impacts patient safety, data integrity, and trial outcomes.
\n\n
What You’ll Do
\n\n
Serve as primary coordinator for assigned clinical trials, managing study activities from start-up through closeout
\nExecute full visit flow independently – participant visits, protocol procedures, data collection, and documentation
\nLead patient interactions with clarity and compassion, ensuring participants feel informed and supported throughout their study experience
\nMaintain accurate, timely, audit-ready documentation across source documents, CRFs, and EDC systems
\nTrack and report adverse events, deviations, and safety findings in accordance with protocol and regulatory requirements
\nCommunicate directly and professionally with investigators, sponsors, CROs, and internal teams
\nSupport site readiness for monitoring visits and audits
\n\n
What We’re Looking For
\nYou’ve got some experience in clinical research and you’re ready for more responsibility. You’re organized, detail-oriented, and comfortable working independently. You take ownership of your work and follow through without being reminded.
\n\n
Bachelor’s degree with 1+ year of relevant experience, OR Associate’s degree with 3+ years of relevant experience, OR High school diploma with 4+ years of relevant experience and at least 1 year of CRC experience
\nExperience performing clinical procedures including vital signs, EKGs, phlebotomy, and lab processing
\nComfortable working independently and managing competing priorities
\nStrong documentation skills and familiarity with EDC platforms and clinical trial management systems
\nPhysical Requirements & Work Environment
\nThis role is performed on-site at a clinical or office facility and requires prolonged periods of sitting, standing, or walking throughout the work environment
\nRequires the ability to communicate clearly in verbal and written forms and to read and interpret detailed materials
\nMust be able to navigate a clinical facility, including areas with limited space, and transport supplies or work materials as needed
\nMay be required to wear personal protective equipment (PPE) in accordance with facility protocols
\nTravel between company sites, meetings, or partner locations may be required
\nReasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the role
\n\n
Why Join Profound Research?
\nMeaningful Impact: Every role at Profound contributes to advancing medical knowledge and expanding therapeutic options for patients – the work we do here matters
\nProfessional Growth: We invest in our people through comprehensive training, certification support, and ongoing education to help you grow in your role and your career
\nLeadership & Advancement: Profound is a place where initiative is recognized. We actively support internal growth and create pathways for people to take on greater responsibility over time
\nCollaborative Culture: You’ll work alongside a team of dedicated professionals who are passionate about clinical research and committed to doing it well
\nFull Benefits Package: Competitive compensation, health insurance, PTO, retirement plan, and professional development support
\nDiverse Clinical Exposure: Work across multiple therapeutic areas and study phases, building a breadth of experience that’s rare in a single organization (for Clinical / Patient-Facing roles)
\nOwn Your Studies. Grow Your Career.
\nIf you’re ready to step into real ownership of clinical trial coordination – managing your own studies, leading patient visits, and working with the independence that comes from having built a strong foundation – this role is the next step.
\n\n
As a Clinical Research Coordinator I at Profound Research, you’ll serve as the primary coordinator for assigned studies at one of our sites. You’ll manage study activities from start-up through closeout, lead interactions with study participants, maintain audit-ready documentation, and work directly with investigators, sponsors, and CROs. This isn’t a support role – you own your studies, and your work directly impacts patient safety, data integrity, and trial outcomes.
\n\n
What You’ll Do
\n\n
Serve as primary coordinator for assigned clinical trials, managing study activities from start-up through closeout
\nExecute full visit flow independently – participant visits, protocol procedures, data collection, and documentation
\nLead patient interactions with clarity and compassion, ensuring participants feel informed and supported throughout their study experience
\nMaintain accurate, timely, audit-ready documentation across source documents, CRFs, and EDC systems
\nTrack and report adverse events, deviations, and safety findings in accordance with protocol and regulatory requirements
\nCommunicate directly and professionally with investigators, sponsors, CROs, and internal teams
\nSupport site readiness for monitoring visits and audits
\n\n
What We’re Looking For
\nYou’ve got some experience in clinical research and you’re ready for more responsibility. You’re organized, detail-oriented, and comfortable working independently. You take ownership of your work and follow through without being reminded.
\n\n
Bachelor’s degree with 1+ year of relevant experience, OR Associate’s degree with 3+ years of relevant experience, OR High school diploma with 4+ years of relevant experience and at least 1 year of CRC experience
\nExperience performing clinical procedures including vital signs, EKGs, phlebotomy, and lab processing
\nComfortable working independently and managing competing priorities
\nStrong documentation skills and familiarity with EDC platforms and clinical trial management systems
\nOwn Your Studies. Grow Your Career.
\nIf you’re ready to step into real ownership of clinical trial coordination – managing your own studies, leading patient visits, and working with the independence that comes from having built a strong foundation – this role is the next step.
\n\n
As a Clinical Research Coordinator I at Profound Research, you’ll serve as the primary coordinator for assigned studies at one of our sites. You’ll manage study activities from start-up through closeout, lead interactions with study participants, maintain audit-ready documentation, and work directly with investigators, sponsors, and CROs. This isn’t a support role – you own your studies, and your work directly impacts patient safety, data integrity, and trial outcomes.
\n\n
What You’ll Do
\n\n
Serve as primary coordinator for assigned clinical trials, managing study activities from start-up through closeout
\nExecute full visit flow independently – participant visits, protocol procedures, data collection, and documentation
\nLead patient interactions with clarity and compassion, ensuring participants feel informed and supported throughout their study experience
\nMaintain accurate, timely, audit-ready documentation across source documents, CRFs, and EDC systems
\nTrack and report adverse events, deviations, and safety findings in accordance with protocol and regulatory requirements
\nCommunicate directly and professionally with investigators, sponsors, CROs, and internal teams
\nSupport site readiness for monitoring visits and audits
\n\n
What We’re Looking For
\nYou’ve got some experience in clinical research and you’re ready for more responsibility. You’re organized, detail-oriented, and comfortable working independently. You take ownership of your work and follow through without being reminded.
\n\n
Bachelor’s degree with 1+ year of relevant experience, OR Associate’s degree with 3+ years of relevant experience, OR High school diploma with 4+ years of relevant experience and at least 1 year of CRC experience
\nExperience performing clinical procedures including vital signs, EKGs, phlebotomy, and lab processing
\nComfortable working independently and managing competing priorities
\nStrong documentation skills and familiarity with EDC platforms and clinical trial management systems
\nPhysical Requirements & Work Environment
\nThis role is performed on-site at a clinical or office facility and requires prolonged periods of sitting, standing, or walking throughout the work environment
\nRequires the ability to communicate clearly in verbal and written forms and to read and interpret detailed materials
\nMust be able to navigate a clinical facility, including areas with limited space, and transport supplies or work materials as needed
\nMay be required to wear personal protective equipment (PPE) in accordance with facility protocols
\nTravel between company sites, meetings, or partner locations may be required
\nReasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the role
\n\n
Why Join Profound Research?
\nMeaningful Impact: Every role at Profound contributes to advancing medical knowledge and expanding therapeutic options for patients – the work we do here matters
\nProfessional Growth: We invest in our people through comprehensive training, certification support, and ongoing education to help you grow in your role and your career
\nLeadership & Advancement: Profound is a place where initiative is recognized. We actively support internal growth and create pathways for people to take on greater responsibility over time
\nCollaborative Culture: You’ll work alongside a team of dedicated professionals who are passionate about clinical research and committed to doing it well
\nFull Benefits Package: Competitive compensation, health insurance, PTO, retirement plan, and professional development support
\nDiverse Clinical Exposure: Work across multiple therapeutic areas and study phases, building a breadth of experience that’s rare in a single organization (for Clinical / Patient-Facing roles)
\nWhy This Role Exists
\nIf you’re curious about how new treatments and vaccines reach patients, detail-oriented by nature, and energized by work that genuinely matters, this is an opportunity to gain hands-on experience in clinical research.
\n\n
As an Assistant Clinical Research Coordinator at Profound Research, you’ll work alongside experienced clinical research staff at one of our sites, supporting the day-to-day execution of high-volume vaccine clinical trials. You’ll learn by doing – gaining hands-on experience in study coordination, patient interaction, data collection, and clinical procedures in a fast-paced, site-based research environment.
\n\n
This is a 1099 contract opportunity to designed to support near-term vaccine study needs, with the potential to convert to a full-time position based on business needs, performance, and role availability. Whether you’re looking to build on prior clinical or research experience or take the next step into the field, this is an opportunity to contribute to meaningful work with a growing organization that values ownership, attention to detail, and patient-centered service.
\n\n
What You’ll Do
\n\n
Support the coordination of high-volume vaccine clinical trials, including patient visits, scheduling, and study-related procedures
\nAssist with data collection and documentation while learning to apply the rigorous standards that clinical research requires
\nPerform and develop competency in clinical procedures including vital signs, EKGs, phlebotomy, and specimen processing
\nHelp prepare for and support efficient participant visits, including rooming patients, organizing supplies, preparing visit materials, and keeping the site team aligned during busy clinic days
\nInteract directly with study participants by greeting them, explaining visit steps, answering process-related questions within scope, and ensuring they feel supported throughout the visit
\nWork closely with Clinical Research Coordinators and site leadership, asking questions, seeking feedback, and building your clinical research knowledge
\nFollow study protocols, SOPs, Good Clinical Practice, Good Documentation Practices, and infection control expectations to support compliant, audit-ready trial execution
\nHelp maintain organized study materials, supplies, documentation, and lab-related workflows needed for patient visits and site operations
\nCommunicate clearly with site team members regarding patient needs, visit flow, documentation status, specimen handling, and study-related tasks
\nContribute to a fast-paced, team-based site environment where quality, urgency, and patient experience all matter
\n\n
What We’re Looking For
\nYou don’t need to have done this exact job before. You need to be the kind of person who takes ownership of their work, communicates clearly, pays close attention to detail, and genuinely cares about the patient experience. The rest we’ll help you build.
\n\n
Essential Qualifications
\nHigh school diploma or technical degree with 3+ years of relevant experience in life sciences, OR Associate’s degree with 1+ year of relevant experience, OR Bachelor’s degree with relevant coursework or experience in a clinical or life sciences setting
\nComfortable working in a fast-paced, team-based environment
\nStrong attention to detail and ability to follow structured processes accurately
\nClear, professional communication with patients, caregivers, clinical staff, and internal team members
\nProficient with standard computer tools; able to learn new systems quickly
\nFamiliarity with medical terminology and basic clinical procedures
\nAbility to maintain professionalism, confidentiality, and care when working with patients and sensitive information
\n\n
Preferred Qualifications
\nPrior clinical research experience, especially in a clinical research coordinator, assistance clinical research coordinator, research assistant, or patient-facing site support role
\nExperience supporting vaccine studies, infectious disease studies, immunization clinics, urgent care, primary care, or other high-volume patient-facing clinical environments
\nExperience with phlebotomy, specimen collection, specimen processing, vital signs, EKGs, or other clinical procedures
\nPrior exposure to Good Clinical Practice, source documentation, regulated healthcare environments, or audit-ready documentation standards
\nExperience using electronic medical records, CTMS platforms, eSource systems, lab portals, or other clinical documentation systems
\n\n
Engagement Details
\nThis is a 1099 independent contractor opportunity designed to support current high-volume vaccine study needs while giving the right person a chance to learn, contribute, and demonstrate readiness for future opportunities. For contractors who perform well and align with business needs, there may be an opportunity to be considered for full-time employment over time.
\n
Why This Role Exists
\nIf you’re curious about how new treatments and vaccines reach patients, detail-oriented by nature, and energized by work that genuinely matters, this is an opportunity to gain hands-on experience in clinical research.
\n\n
As an Assistant Clinical Research Coordinator at Profound Research, you’ll work alongside experienced clinical research staff at one of our sites, supporting the day-to-day execution of high-volume vaccine clinical trials. You’ll learn by doing – gaining hands-on experience in study coordination, patient interaction, data collection, and clinical procedures in a fast-paced, site-based research environment.
\n\n
This is a 1099 contract opportunity to designed to support near-term vaccine study needs, with the potential to convert to a full-time position based on business needs, performance, and role availability. Whether you’re looking to build on prior clinical or research experience or take the next step into the field, this is an opportunity to contribute to meaningful work with a growing organization that values ownership, attention to detail, and patient-centered service.
\n\n
What You’ll Do
\n\n
Support the coordination of high-volume vaccine clinical trials, including patient visits, scheduling, and study-related procedures
\nAssist with data collection and documentation while learning to apply the rigorous standards that clinical research requires
\nPerform and develop competency in clinical procedures including vital signs, EKGs, phlebotomy, and specimen processing
\nHelp prepare for and support efficient participant visits, including rooming patients, organizing supplies, preparing visit materials, and keeping the site team aligned during busy clinic days
\nInteract directly with study participants by greeting them, explaining visit steps, answering process-related questions within scope, and ensuring they feel supported throughout the visit
\nWork closely with Clinical Research Coordinators and site leadership, asking questions, seeking feedback, and building your clinical research knowledge
\nFollow study protocols, SOPs, Good Clinical Practice, Good Documentation Practices, and infection control expectations to support compliant, audit-ready trial execution
\nHelp maintain organized study materials, supplies, documentation, and lab-related workflows needed for patient visits and site operations
\nCommunicate clearly with site team members regarding patient needs, visit flow, documentation status, specimen handling, and study-related tasks
\nContribute to a fast-paced, team-based site environment where quality, urgency, and patient experience all matter
\n\n
What We’re Looking For
\nYou don’t need to have done this exact job before. You need to be the kind of person who takes ownership of their work, communicates clearly, pays close attention to detail, and genuinely cares about the patient experience. The rest we’ll help you build.
\n\n
Essential Qualifications
\nHigh school diploma or technical degree with 3+ years of relevant experience in life sciences, OR Associate’s degree with 1+ year of relevant experience, OR Bachelor’s degree with relevant coursework or experience in a clinical or life sciences setting
\nComfortable working in a fast-paced, team-based environment
\nStrong attention to detail and ability to follow structured processes accurately
\nClear, professional communication with patients, caregivers, clinical staff, and internal team members
\nProficient with standard computer tools; able to learn new systems quickly
\nFamiliarity with medical terminology and basic clinical procedures
\nAbility to maintain professionalism, confidentiality, and care when working with patients and sensitive information
\n\n
Preferred Qualifications
\nPrior clinical research experience, especially in a clinical research coordinator, assistance clinical research coordinator, research assistant, or patient-facing site support role
\nExperience supporting vaccine studies, infectious disease studies, immunization clinics, urgent care, primary care, or other high-volume patient-facing clinical environments
\nExperience with phlebotomy, specimen collection, specimen processing, vital signs, EKGs, or other clinical procedures
\nPrior exposure to Good Clinical Practice, source documentation, regulated healthcare environments, or audit-ready documentation standards
\nExperience using electronic medical records, CTMS platforms, eSource systems, lab portals, or other clinical documentation systems
\n\n
Engagement Details
\nThis is a 1099 independent contractor opportunity designed to support current high-volume vaccine study needs while giving the right person a chance to learn, contribute, and demonstrate readiness for future opportunities. For contractors who perform well and align with business needs, there may be an opportunity to be considered for full-time employment over time.
\n
Physical Requirements & Work Environment
\nThis role is performed on-site at a clinical or office facility and requires prolonged periods of sitting, standing, or walking throughout the work environment
\nRequires the ability to communicate clearly in verbal and written forms and to read and interpret detailed materials
\nMust be able to navigate a clinical facility, including areas with limited space, and transport supplies or work materials as needed
\nMay be required to wear personal protective equipment (PPE) in accordance with facility protocols
\nTravel between company sites, meetings, or partner locations may be required
\nReasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the role
\n\n
Why Join Profound Research?
\nMeaningful Impact: Every role at Profound contributes to advancing medical knowledge and expanding therapeutic options for patients – the work we do here matters
\nProfessional Growth: We invest in our people through comprehensive training, certification support, and ongoing education to help you grow in your role and your career
\nLeadership & Advancement: Profound is a place where initiative is recognized. We actively support internal growth and create pathways for people to take on greater responsibility over time
\nCollaborative Culture: You’ll work alongside a team of dedicated professionals who are passionate about clinical research and committed to doing it well
\nFull Benefits Package: Competitive compensation, health insurance, PTO, retirement plan, and professional development support
\nDiverse Clinical Exposure: Work across multiple therapeutic areas and study phases, building a breadth of experience that’s rare in a single organization (for Clinical / Patient-Facing roles)
\nWhy This Role Exists
\nIf you’re curious about how new treatments and vaccines reach patients, detail-oriented by nature, and energized by work that genuinely matters, this is an opportunity to gain hands-on experience in clinical research.
\n\n
As an Assistant Clinical Research Coordinator at Profound Research, you’ll work alongside experienced clinical research staff at one of our sites, supporting the day-to-day execution of high-volume vaccine clinical trials. You’ll learn by doing – gaining hands-on experience in study coordination, patient interaction, data collection, and clinical procedures in a fast-paced, site-based research environment.
\n\n
This is a 1099 contract opportunity to designed to support near-term vaccine study needs, with the potential to convert to a full-time position based on business needs, performance, and role availability. Whether you’re looking to build on prior clinical or research experience or take the next step into the field, this is an opportunity to contribute to meaningful work with a growing organization that values ownership, attention to detail, and patient-centered service.
\n\n
What You’ll Do
\n\n
Support the coordination of high-volume vaccine clinical trials, including patient visits, scheduling, and study-related procedures
\nAssist with data collection and documentation while learning to apply the rigorous standards that clinical research requires
\nPerform and develop competency in clinical procedures including vital signs, EKGs, phlebotomy, and specimen processing
\nHelp prepare for and support efficient participant visits, including rooming patients, organizing supplies, preparing visit materials, and keeping the site team aligned during busy clinic days
\nInteract directly with study participants by greeting them, explaining visit steps, answering process-related questions within scope, and ensuring they feel supported throughout the visit
\nWork closely with Clinical Research Coordinators and site leadership, asking questions, seeking feedback, and building your clinical research knowledge
\nFollow study protocols, SOPs, Good Clinical Practice, Good Documentation Practices, and infection control expectations to support compliant, audit-ready trial execution
\nHelp maintain organized study materials, supplies, documentation, and lab-related workflows needed for patient visits and site operations
\nCommunicate clearly with site team members regarding patient needs, visit flow, documentation status, specimen handling, and study-related tasks
\nContribute to a fast-paced, team-based site environment where quality, urgency, and patient experience all matter
\n\n
What We’re Looking For
\nYou don’t need to have done this exact job before. You need to be the kind of person who takes ownership of their work, communicates clearly, pays close attention to detail, and genuinely cares about the patient experience. The rest we’ll help you build.
\n\n
Essential Qualifications
\nHigh school diploma or technical degree with 3+ years of relevant experience in life sciences, OR Associate’s degree with 1+ year of relevant experience, OR Bachelor’s degree with relevant coursework or experience in a clinical or life sciences setting
\nComfortable working in a fast-paced, team-based environment
\nStrong attention to detail and ability to follow structured processes accurately
\nClear, professional communication with patients, caregivers, clinical staff, and internal team members
\nProficient with standard computer tools; able to learn new systems quickly
\nFamiliarity with medical terminology and basic clinical procedures
\nAbility to maintain professionalism, confidentiality, and care when working with patients and sensitive information
\n\n
Preferred Qualifications
\nPrior clinical research experience, especially in a clinical research coordinator, assistance clinical research coordinator, research assistant, or patient-facing site support role
\nExperience supporting vaccine studies, infectious disease studies, immunization clinics, urgent care, primary care, or other high-volume patient-facing clinical environments
\nExperience with phlebotomy, specimen collection, specimen processing, vital signs, EKGs, or other clinical procedures
\nPrior exposure to Good Clinical Practice, source documentation, regulated healthcare environments, or audit-ready documentation standards
\nExperience using electronic medical records, CTMS platforms, eSource systems, lab portals, or other clinical documentation systems
\n\n
Engagement Details
\nThis is a 1099 independent contractor opportunity designed to support current high-volume vaccine study needs while giving the right person a chance to learn, contribute, and demonstrate readiness for future opportunities. For contractors who perform well and align with business needs, there may be an opportunity to be considered for full-time employment over time.
\n
Why This Role Exists
\nIf you’re curious about how new treatments and vaccines reach patients, detail-oriented by nature, and energized by work that genuinely matters, this is an opportunity to gain hands-on experience in clinical research.
\n\n
As an Assistant Clinical Research Coordinator at Profound Research, you’ll work alongside experienced clinical research staff at one of our sites, supporting the day-to-day execution of high-volume vaccine clinical trials. You’ll learn by doing – gaining hands-on experience in study coordination, patient interaction, data collection, and clinical procedures in a fast-paced, site-based research environment.
\n\n
This is a 1099 contract opportunity to designed to support near-term vaccine study needs, with the potential to convert to a full-time position based on business needs, performance, and role availability. Whether you’re looking to build on prior clinical or research experience or take the next step into the field, this is an opportunity to contribute to meaningful work with a growing organization that values ownership, attention to detail, and patient-centered service.
\n\n
What You’ll Do
\n\n
Support the coordination of high-volume vaccine clinical trials, including patient visits, scheduling, and study-related procedures
\nAssist with data collection and documentation while learning to apply the rigorous standards that clinical research requires
\nPerform and develop competency in clinical procedures including vital signs, EKGs, phlebotomy, and specimen processing
\nHelp prepare for and support efficient participant visits, including rooming patients, organizing supplies, preparing visit materials, and keeping the site team aligned during busy clinic days
\nInteract directly with study participants by greeting them, explaining visit steps, answering process-related questions within scope, and ensuring they feel supported throughout the visit
\nWork closely with Clinical Research Coordinators and site leadership, asking questions, seeking feedback, and building your clinical research knowledge
\nFollow study protocols, SOPs, Good Clinical Practice, Good Documentation Practices, and infection control expectations to support compliant, audit-ready trial execution
\nHelp maintain organized study materials, supplies, documentation, and lab-related workflows needed for patient visits and site operations
\nCommunicate clearly with site team members regarding patient needs, visit flow, documentation status, specimen handling, and study-related tasks
\nContribute to a fast-paced, team-based site environment where quality, urgency, and patient experience all matter
\n\n
What We’re Looking For
\nYou don’t need to have done this exact job before. You need to be the kind of person who takes ownership of their work, communicates clearly, pays close attention to detail, and genuinely cares about the patient experience. The rest we’ll help you build.
\n\n
Essential Qualifications
\nHigh school diploma or technical degree with 3+ years of relevant experience in life sciences, OR Associate’s degree with 1+ year of relevant experience, OR Bachelor’s degree with relevant coursework or experience in a clinical or life sciences setting
\nComfortable working in a fast-paced, team-based environment
\nStrong attention to detail and ability to follow structured processes accurately
\nClear, professional communication with patients, caregivers, clinical staff, and internal team members
\nProficient with standard computer tools; able to learn new systems quickly
\nFamiliarity with medical terminology and basic clinical procedures
\nAbility to maintain professionalism, confidentiality, and care when working with patients and sensitive information
\n\n
Preferred Qualifications
\nPrior clinical research experience, especially in a clinical research coordinator, assistance clinical research coordinator, research assistant, or patient-facing site support role
\nExperience supporting vaccine studies, infectious disease studies, immunization clinics, urgent care, primary care, or other high-volume patient-facing clinical environments
\nExperience with phlebotomy, specimen collection, specimen processing, vital signs, EKGs, or other clinical procedures
\nPrior exposure to Good Clinical Practice, source documentation, regulated healthcare environments, or audit-ready documentation standards
\nExperience using electronic medical records, CTMS platforms, eSource systems, lab portals, or other clinical documentation systems
\n\n
Engagement Details
\nThis is a 1099 independent contractor opportunity designed to support current high-volume vaccine study needs while giving the right person a chance to learn, contribute, and demonstrate readiness for future opportunities. For contractors who perform well and align with business needs, there may be an opportunity to be considered for full-time employment over time.
\n
Physical Requirements & Work Environment
\nThis role is performed on-site at a clinical or office facility and requires prolonged periods of sitting, standing, or walking throughout the work environment
\nRequires the ability to communicate clearly in verbal and written forms and to read and interpret detailed materials
\nMust be able to navigate a clinical facility, including areas with limited space, and transport supplies or work materials as needed
\nMay be required to wear personal protective equipment (PPE) in accordance with facility protocols
\nTravel between company sites, meetings, or partner locations may be required
\nReasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the role
\n\n
Why Join Profound Research?
\nMeaningful Impact: Every role at Profound contributes to advancing medical knowledge and expanding therapeutic options for patients – the work we do here matters
\nProfessional Growth: We invest in our people through comprehensive training, certification support, and ongoing education to help you grow in your role and your career
\nLeadership & Advancement: Profound is a place where initiative is recognized. We actively support internal growth and create pathways for people to take on greater responsibility over time
\nCollaborative Culture: You’ll work alongside a team of dedicated professionals who are passionate about clinical research and committed to doing it well
\nFull Benefits Package: Competitive compensation, health insurance, PTO, retirement plan, and professional development support
\nDiverse Clinical Exposure: Work across multiple therapeutic areas and study phases, building a breadth of experience that’s rare in a single organization (for Clinical / Patient-Facing roles)
\nWhy This Role Exists
\nIf you’re curious about how new treatments and vaccines reach patients, detail-oriented by nature, and energized by work that genuinely matters, this is an opportunity to gain hands-on experience in clinical research.
\n\n
As an Assistant Clinical Research Coordinator at Profound Research, you’ll work alongside experienced clinical research staff at one of our sites, supporting the day-to-day execution of high-volume vaccine clinical trials. You’ll learn by doing – gaining hands-on experience in study coordination, patient interaction, data collection, and clinical procedures in a fast-paced, site-based research environment.
\n\n
This is a 1099 contract opportunity to designed to support near-term vaccine study needs, with the potential to convert to a full-time position based on business needs, performance, and role availability. Whether you’re looking to build on prior clinical or research experience or take the next step into the field, this is an opportunity to contribute to meaningful work with a growing organization that values ownership, attention to detail, and patient-centered service.
\n\n
What You’ll Do
\n\n
Support the coordination of high-volume vaccine clinical trials, including patient visits, scheduling, and study-related procedures
\nAssist with data collection and documentation while learning to apply the rigorous standards that clinical research requires
\nPerform and develop competency in clinical procedures including vital signs, EKGs, phlebotomy, and specimen processing
\nHelp prepare for and support efficient participant visits, including rooming patients, organizing supplies, preparing visit materials, and keeping the site team aligned during busy clinic days
\nInteract directly with study participants by greeting them, explaining visit steps, answering process-related questions within scope, and ensuring they feel supported throughout the visit
\nWork closely with Clinical Research Coordinators and site leadership, asking questions, seeking feedback, and building your clinical research knowledge
\nFollow study protocols, SOPs, Good Clinical Practice, Good Documentation Practices, and infection control expectations to support compliant, audit-ready trial execution
\nHelp maintain organized study materials, supplies, documentation, and lab-related workflows needed for patient visits and site operations
\nCommunicate clearly with site team members regarding patient needs, visit flow, documentation status, specimen handling, and study-related tasks
\nContribute to a fast-paced, team-based site environment where quality, urgency, and patient experience all matter
\n\n
What We’re Looking For
\nYou don’t need to have done this exact job before. You need to be the kind of person who takes ownership of their work, communicates clearly, pays close attention to detail, and genuinely cares about the patient experience. The rest we’ll help you build.
\n\n
Essential Qualifications
\nHigh school diploma or technical degree with 3+ years of relevant experience in life sciences, OR Associate’s degree with 1+ year of relevant experience, OR Bachelor’s degree with relevant coursework or experience in a clinical or life sciences setting
\nComfortable working in a fast-paced, team-based environment
\nStrong attention to detail and ability to follow structured processes accurately
\nClear, professional communication with patients, caregivers, clinical staff, and internal team members
\nProficient with standard computer tools; able to learn new systems quickly
\nFamiliarity with medical terminology and basic clinical procedures
\nAbility to maintain professionalism, confidentiality, and care when working with patients and sensitive information
\n\n
Preferred Qualifications
\nPrior clinical research experience, especially in a clinical research coordinator, assistance clinical research coordinator, research assistant, or patient-facing site support role
\nExperience supporting vaccine studies, infectious disease studies, immunization clinics, urgent care, primary care, or other high-volume patient-facing clinical environments
\nExperience with phlebotomy, specimen collection, specimen processing, vital signs, EKGs, or other clinical procedures
\nPrior exposure to Good Clinical Practice, source documentation, regulated healthcare environments, or audit-ready documentation standards
\nExperience using electronic medical records, CTMS platforms, eSource systems, lab portals, or other clinical documentation systems
\n\n
Engagement Details
\nThis is a 1099 independent contractor opportunity designed to support current high-volume vaccine study needs while giving the right person a chance to learn, contribute, and demonstrate readiness for future opportunities. For contractors who perform well and align with business needs, there may be an opportunity to be considered for full-time employment over time.
\n
Why This Role Exists
\nIf you’re curious about how new treatments and vaccines reach patients, detail-oriented by nature, and energized by work that genuinely matters, this is an opportunity to gain hands-on experience in clinical research.
\n\n
As an Assistant Clinical Research Coordinator at Profound Research, you’ll work alongside experienced clinical research staff at one of our sites, supporting the day-to-day execution of high-volume vaccine clinical trials. You’ll learn by doing – gaining hands-on experience in study coordination, patient interaction, data collection, and clinical procedures in a fast-paced, site-based research environment.
\n\n
This is a 1099 contract opportunity to designed to support near-term vaccine study needs, with the potential to convert to a full-time position based on business needs, performance, and role availability. Whether you’re looking to build on prior clinical or research experience or take the next step into the field, this is an opportunity to contribute to meaningful work with a growing organization that values ownership, attention to detail, and patient-centered service.
\n\n
What You’ll Do
\n\n
Support the coordination of high-volume vaccine clinical trials, including patient visits, scheduling, and study-related procedures
\nAssist with data collection and documentation while learning to apply the rigorous standards that clinical research requires
\nPerform and develop competency in clinical procedures including vital signs, EKGs, phlebotomy, and specimen processing
\nHelp prepare for and support efficient participant visits, including rooming patients, organizing supplies, preparing visit materials, and keeping the site team aligned during busy clinic days
\nInteract directly with study participants by greeting them, explaining visit steps, answering process-related questions within scope, and ensuring they feel supported throughout the visit
\nWork closely with Clinical Research Coordinators and site leadership, asking questions, seeking feedback, and building your clinical research knowledge
\nFollow study protocols, SOPs, Good Clinical Practice, Good Documentation Practices, and infection control expectations to support compliant, audit-ready trial execution
\nHelp maintain organized study materials, supplies, documentation, and lab-related workflows needed for patient visits and site operations
\nCommunicate clearly with site team members regarding patient needs, visit flow, documentation status, specimen handling, and study-related tasks
\nContribute to a fast-paced, team-based site environment where quality, urgency, and patient experience all matter
\n\n
What We’re Looking For
\nYou don’t need to have done this exact job before. You need to be the kind of person who takes ownership of their work, communicates clearly, pays close attention to detail, and genuinely cares about the patient experience. The rest we’ll help you build.
\n\n
Essential Qualifications
\nHigh school diploma or technical degree with 3+ years of relevant experience in life sciences, OR Associate’s degree with 1+ year of relevant experience, OR Bachelor’s degree with relevant coursework or experience in a clinical or life sciences setting
\nComfortable working in a fast-paced, team-based environment
\nStrong attention to detail and ability to follow structured processes accurately
\nClear, professional communication with patients, caregivers, clinical staff, and internal team members
\nProficient with standard computer tools; able to learn new systems quickly
\nFamiliarity with medical terminology and basic clinical procedures
\nAbility to maintain professionalism, confidentiality, and care when working with patients and sensitive information
\n\n
Preferred Qualifications
\nPrior clinical research experience, especially in a clinical research coordinator, assistance clinical research coordinator, research assistant, or patient-facing site support role
\nExperience supporting vaccine studies, infectious disease studies, immunization clinics, urgent care, primary care, or other high-volume patient-facing clinical environments
\nExperience with phlebotomy, specimen collection, specimen processing, vital signs, EKGs, or other clinical procedures
\nPrior exposure to Good Clinical Practice, source documentation, regulated healthcare environments, or audit-ready documentation standards
\nExperience using electronic medical records, CTMS platforms, eSource systems, lab portals, or other clinical documentation systems
\n\n
Engagement Details
\nThis is a 1099 independent contractor opportunity designed to support current high-volume vaccine study needs while giving the right person a chance to learn, contribute, and demonstrate readiness for future opportunities. For contractors who perform well and align with business needs, there may be an opportunity to be considered for full-time employment over time.
\n
Physical Requirements & Work Environment
\nThis role is performed on-site at a clinical or office facility and requires prolonged periods of sitting, standing, or walking throughout the work environment
\nRequires the ability to communicate clearly in verbal and written forms and to read and interpret detailed materials
\nMust be able to navigate a clinical facility, including areas with limited space, and transport supplies or work materials as needed
\nMay be required to wear personal protective equipment (PPE) in accordance with facility protocols
\nTravel between company sites, meetings, or partner locations may be required
\nReasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the role
\n\n
Why Join Profound Research?
\nMeaningful Impact: Every role at Profound contributes to advancing medical knowledge and expanding therapeutic options for patients – the work we do here matters
\nProfessional Growth: We invest in our people through comprehensive training, certification support, and ongoing education to help you grow in your role and your career
\nLeadership & Advancement: Profound is a place where initiative is recognized. We actively support internal growth and create pathways for people to take on greater responsibility over time
\nCollaborative Culture: You’ll work alongside a team of dedicated professionals who are passionate about clinical research and committed to doing it well
\nFull Benefits Package: Competitive compensation, health insurance, PTO, retirement plan, and professional development support
\nDiverse Clinical Exposure: Work across multiple therapeutic areas and study phases, building a breadth of experience that’s rare in a single organization (for Clinical / Patient-Facing roles)
\nWhy This Role Exists
\nIf you’re ready to bring your clinical research experience into a fast-paced, high-volume environment, this role offers an opportunity to make an immediate impact.
\n\n
As a Clinical Research Coordinator I at Profound Research, you’ll support the execution of high-volume vaccine clinical trials at one of our sites. You’ll help manage study activities, lead participant visits, complete protocol-required procedures and documentation, and work closely with investigators, sponsors, CROs, and internal teams. This is not an entry-level support role – you’ll be expected to operate with ownership, sound judgment, and a strong understanding of clinical research standards.
\n\n
This is a 1099 contract opportunity designed to support near-term vaccine study needs, with the potential to convert to a full-time position based on business needs, performance, and role availability. If you’re looking to build on your clinical research experience with a growing organization that values accountability, quality, and patient-centered execution, we’d like to hear from you.
\n\n
What You’ll Do
\n\n
Serve as a coordinator for assigned vaccine clinical trials, supporting study activities from start-up through closeout as needed
\nExecute participant visit flow independently, including visit preparation, patient interaction, protocol-related procedures, data collection, and documentation
\nSupport high-volume clinic days by helping maintain efficient visit flow, clear communication, and accurate completion of study-required tasks
\nLead patient interactions with clarity and compassion, ensuring participants feel informed and supported throughout their study experience
\nPerform clinical procedures as required by protocol, which may include vital signs, EKGs, phlebotomy, specimen collection, specimen processing, and other study-specific assessments
\nMaintain accurate, timely, audit-ready documentation across source documents, CRFs, EDC systems, CTMS platforms, and other study tools
\nTrack, document, and escalate adverse events, deviations, safety findings, and protocol-related issues in accordance with study and regulatory requirements
\nCommunicate directly and professionally with investigators, sponsors, CROs, monitors, vendors, and internal team members
\nSupport site readiness for monitoring visits, sponsor communications, internal quality review, and audits
\nFollow study protocols, SOPs, Good Clinical Practice, Good Documentation Practices, and infection control expectations to support compliant, high-quality trial execution
\nHelp maintain organized study materials, lab workflows, visit supplies, and documentation needed for efficient site operations
\nContribute to a fast-paced, team-based environment where quality, urgency, patient experience, and data integrity all matter
\n\n
What We’re Looking For
\nYou have clinical research experience and are ready to operate with more ownership. You’re organized, detail-oriented, comfortable managing competing priorities, and able to follow through without heavy oversight.
\n\n
Essential Qualifications
\nBachelor’s degree with 1+ year of relevant experience, OR Associate’s degree with 3+ years of relevant experience, OR High school diploma with 4+ years of relevant experience and at least 1 year of CRC experience
\nPrior experience in clinical research, including exposure to clinical trial coordination, study visits, source documentation, and protocol-driven workflows
\nExperience performing or supporting clinical procedures, which may include vital signs, EKGs, phlebotomy, specimen collection, specimen processing, or lab-related workflows
\nComfortable working independently in a fast-paced, site-based clinical research environment
\nAbility to support high-volume patient visits while maintaining accuracy, professionalism, and a patient-centered approach
\nStrong documentation skills and understanding of audit-ready clinical research standards
\nFamiliarity with EDC platforms, clinical trial management systems, eSource tools, EMRs, lab portals, or other clinical documentation systems
\nWorking knowledge of Good Clinical Practice, Good Documentation Practices, protocol adherence, and regulatory expectations
\nStrong communication skills with the ability to interact professionally with patients, caregivers, investigators, site staff, sponsors, CROs, monitors, and internal teams
\nAbility to maintain professionalism, confidentiality, and care when working with patients and sensitive information
\n\n
Preferred Qualifications
\nExperience supporting vaccine studies, infectious disease studies, immunization clinics, urgent care, primary care, or other high-volume patient-facing clinical environments
\nPrior experience serving as a primary or lead coordinator for assigned studies
\nExperience with adverse event documentation, protocol deviations, query resolution, monitoring visits, and sponsor/CRO communication
\nActive or prior ICH-GCP, IATA, phlebotomy, or related clinical research certifications
\nExperience supporting start-up, closeout, or audit/monitoring readiness activities
\nComfort adapting quickly to study-specific workflows, systems, and enrollment timelines
\n\n
Engagement Details
\nThis is a 1099 independent contractor opportunity designed to support current high-volume vaccine study needs while giving the right person a chance to learn, contribute quickly, demonstrate ownership, and be considered for future opportunities. For contractors who perform well and align with business needs, there may be an opportunity to be considered for full-time employment over time.
\nWhy This Role Exists
\nIf you’re ready to bring your clinical research experience into a fast-paced, high-volume environment, this role offers an opportunity to make an immediate impact.
\n\n
As a Clinical Research Coordinator I at Profound Research, you’ll support the execution of high-volume vaccine clinical trials at one of our sites. You’ll help manage study activities, lead participant visits, complete protocol-required procedures and documentation, and work closely with investigators, sponsors, CROs, and internal teams. This is not an entry-level support role – you’ll be expected to operate with ownership, sound judgment, and a strong understanding of clinical research standards.
\n\n
This is a 1099 contract opportunity designed to support near-term vaccine study needs, with the potential to convert to a full-time position based on business needs, performance, and role availability. If you’re looking to build on your clinical research experience with a growing organization that values accountability, quality, and patient-centered execution, we’d like to hear from you.
\n\n
What You’ll Do
\n\n
Serve as a coordinator for assigned vaccine clinical trials, supporting study activities from start-up through closeout as needed
\nExecute participant visit flow independently, including visit preparation, patient interaction, protocol-related procedures, data collection, and documentation
\nSupport high-volume clinic days by helping maintain efficient visit flow, clear communication, and accurate completion of study-required tasks
\nLead patient interactions with clarity and compassion, ensuring participants feel informed and supported throughout their study experience
\nPerform clinical procedures as required by protocol, which may include vital signs, EKGs, phlebotomy, specimen collection, specimen processing, and other study-specific assessments
\nMaintain accurate, timely, audit-ready documentation across source documents, CRFs, EDC systems, CTMS platforms, and other study tools
\nTrack, document, and escalate adverse events, deviations, safety findings, and protocol-related issues in accordance with study and regulatory requirements
\nCommunicate directly and professionally with investigators, sponsors, CROs, monitors, vendors, and internal team members
\nSupport site readiness for monitoring visits, sponsor communications, internal quality review, and audits
\nFollow study protocols, SOPs, Good Clinical Practice, Good Documentation Practices, and infection control expectations to support compliant, high-quality trial execution
\nHelp maintain organized study materials, lab workflows, visit supplies, and documentation needed for efficient site operations
\nContribute to a fast-paced, team-based environment where quality, urgency, patient experience, and data integrity all matter
\n\n
What We’re Looking For
\nYou have clinical research experience and are ready to operate with more ownership. You’re organized, detail-oriented, comfortable managing competing priorities, and able to follow through without heavy oversight.
\n\n
Essential Qualifications
\nBachelor’s degree with 1+ year of relevant experience, OR Associate’s degree with 3+ years of relevant experience, OR High school diploma with 4+ years of relevant experience and at least 1 year of CRC experience
\nPrior experience in clinical research, including exposure to clinical trial coordination, study visits, source documentation, and protocol-driven workflows
\nExperience performing or supporting clinical procedures, which may include vital signs, EKGs, phlebotomy, specimen collection, specimen processing, or lab-related workflows
\nComfortable working independently in a fast-paced, site-based clinical research environment
\nAbility to support high-volume patient visits while maintaining accuracy, professionalism, and a patient-centered approach
\nStrong documentation skills and understanding of audit-ready clinical research standards
\nFamiliarity with EDC platforms, clinical trial management systems, eSource tools, EMRs, lab portals, or other clinical documentation systems
\nWorking knowledge of Good Clinical Practice, Good Documentation Practices, protocol adherence, and regulatory expectations
\nStrong communication skills with the ability to interact professionally with patients, caregivers, investigators, site staff, sponsors, CROs, monitors, and internal teams
\nAbility to maintain professionalism, confidentiality, and care when working with patients and sensitive information
\n\n
Preferred Qualifications
\nExperience supporting vaccine studies, infectious disease studies, immunization clinics, urgent care, primary care, or other high-volume patient-facing clinical environments
\nPrior experience serving as a primary or lead coordinator for assigned studies
\nExperience with adverse event documentation, protocol deviations, query resolution, monitoring visits, and sponsor/CRO communication
\nActive or prior ICH-GCP, IATA, phlebotomy, or related clinical research certifications
\nExperience supporting start-up, closeout, or audit/monitoring readiness activities
\nComfort adapting quickly to study-specific workflows, systems, and enrollment timelines
\n\n
Engagement Details
\nThis is a 1099 independent contractor opportunity designed to support current high-volume vaccine study needs while giving the right person a chance to learn, contribute quickly, demonstrate ownership, and be considered for future opportunities. For contractors who perform well and align with business needs, there may be an opportunity to be considered for full-time employment over time.
\nPhysical Requirements & Work Environment
\nThis role is performed on-site at a clinical or office facility and requires prolonged periods of sitting, standing, or walking throughout the work environment
\nRequires the ability to communicate clearly in verbal and written forms and to read and interpret detailed materials
\nMust be able to navigate a clinical facility, including areas with limited space, and transport supplies or work materials as needed
\nMay be required to wear personal protective equipment (PPE) in accordance with facility protocols
\nTravel between company sites, meetings, or partner locations may be required
\nReasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the role
\n\n
Why Join Profound Research?
\nMeaningful Impact: Every role at Profound contributes to advancing medical knowledge and expanding therapeutic options for patients – the work we do here matters
\nProfessional Growth: We invest in our people through comprehensive training, certification support, and ongoing education to help you grow in your role and your career
\nLeadership & Advancement: Profound is a place where initiative is recognized. We actively support internal growth and create pathways for people to take on greater responsibility over time
\nCollaborative Culture: You’ll work alongside a team of dedicated professionals who are passionate about clinical research and committed to doing it well
\nFull Benefits Package: Competitive compensation, health insurance, PTO, retirement plan, and professional development support
\nDiverse Clinical Exposure: Work across multiple therapeutic areas and study phases, building a breadth of experience that’s rare in a single organization (for Clinical / Patient-Facing roles)
\nWhy This Role Exists
\nIf you’re ready to bring your clinical research experience into a fast-paced, high-volume environment, this role offers an opportunity to make an immediate impact.
\n\n
As a Clinical Research Coordinator I at Profound Research, you’ll support the execution of high-volume vaccine clinical trials at one of our sites. You’ll help manage study activities, lead participant visits, complete protocol-required procedures and documentation, and work closely with investigators, sponsors, CROs, and internal teams. This is not an entry-level support role – you’ll be expected to operate with ownership, sound judgment, and a strong understanding of clinical research standards.
\n\n
This is a 1099 contract opportunity designed to support near-term vaccine study needs, with the potential to convert to a full-time position based on business needs, performance, and role availability. If you’re looking to build on your clinical research experience with a growing organization that values accountability, quality, and patient-centered execution, we’d like to hear from you.
\n\n
What You’ll Do
\n\n
Serve as a coordinator for assigned vaccine clinical trials, supporting study activities from start-up through closeout as needed
\nExecute participant visit flow independently, including visit preparation, patient interaction, protocol-related procedures, data collection, and documentation
\nSupport high-volume clinic days by helping maintain efficient visit flow, clear communication, and accurate completion of study-required tasks
\nLead patient interactions with clarity and compassion, ensuring participants feel informed and supported throughout their study experience
\nPerform clinical procedures as required by protocol, which may include vital signs, EKGs, phlebotomy, specimen collection, specimen processing, and other study-specific assessments
\nMaintain accurate, timely, audit-ready documentation across source documents, CRFs, EDC systems, CTMS platforms, and other study tools
\nTrack, document, and escalate adverse events, deviations, safety findings, and protocol-related issues in accordance with study and regulatory requirements
\nCommunicate directly and professionally with investigators, sponsors, CROs, monitors, vendors, and internal team members
\nSupport site readiness for monitoring visits, sponsor communications, internal quality review, and audits
\nFollow study protocols, SOPs, Good Clinical Practice, Good Documentation Practices, and infection control expectations to support compliant, high-quality trial execution
\nHelp maintain organized study materials, lab workflows, visit supplies, and documentation needed for efficient site operations
\nContribute to a fast-paced, team-based environment where quality, urgency, patient experience, and data integrity all matter
\n\n
What We’re Looking For
\nYou have clinical research experience and are ready to operate with more ownership. You’re organized, detail-oriented, comfortable managing competing priorities, and able to follow through without heavy oversight.
\n\n
Essential Qualifications
\nBachelor’s degree with 1+ year of relevant experience, OR Associate’s degree with 3+ years of relevant experience, OR High school diploma with 4+ years of relevant experience and at least 1 year of CRC experience
\nPrior experience in clinical research, including exposure to clinical trial coordination, study visits, source documentation, and protocol-driven workflows
\nExperience performing or supporting clinical procedures, which may include vital signs, EKGs, phlebotomy, specimen collection, specimen processing, or lab-related workflows
\nComfortable working independently in a fast-paced, site-based clinical research environment
\nAbility to support high-volume patient visits while maintaining accuracy, professionalism, and a patient-centered approach
\nStrong documentation skills and understanding of audit-ready clinical research standards
\nFamiliarity with EDC platforms, clinical trial management systems, eSource tools, EMRs, lab portals, or other clinical documentation systems
\nWorking knowledge of Good Clinical Practice, Good Documentation Practices, protocol adherence, and regulatory expectations
\nStrong communication skills with the ability to interact professionally with patients, caregivers, investigators, site staff, sponsors, CROs, monitors, and internal teams
\nAbility to maintain professionalism, confidentiality, and care when working with patients and sensitive information
\n\n
Preferred Qualifications
\nExperience supporting vaccine studies, infectious disease studies, immunization clinics, urgent care, primary care, or other high-volume patient-facing clinical environments
\nPrior experience serving as a primary or lead coordinator for assigned studies
\nExperience with adverse event documentation, protocol deviations, query resolution, monitoring visits, and sponsor/CRO communication
\nActive or prior ICH-GCP, IATA, phlebotomy, or related clinical research certifications
\nExperience supporting start-up, closeout, or audit/monitoring readiness activities
\nComfort adapting quickly to study-specific workflows, systems, and enrollment timelines
\n\n
Engagement Details
\nThis is a 1099 independent contractor opportunity designed to support current high-volume vaccine study needs while giving the right person a chance to learn, contribute quickly, demonstrate ownership, and be considered for future opportunities. For contractors who perform well and align with business needs, there may be an opportunity to be considered for full-time employment over time.
\nWhy This Role Exists
\nIf you’re ready to bring your clinical research experience into a fast-paced, high-volume environment, this role offers an opportunity to make an immediate impact.
\n\n
As a Clinical Research Coordinator I at Profound Research, you’ll support the execution of high-volume vaccine clinical trials at one of our sites. You’ll help manage study activities, lead participant visits, complete protocol-required procedures and documentation, and work closely with investigators, sponsors, CROs, and internal teams. This is not an entry-level support role – you’ll be expected to operate with ownership, sound judgment, and a strong understanding of clinical research standards.
\n\n
This is a 1099 contract opportunity designed to support near-term vaccine study needs, with the potential to convert to a full-time position based on business needs, performance, and role availability. If you’re looking to build on your clinical research experience with a growing organization that values accountability, quality, and patient-centered execution, we’d like to hear from you.
\n\n
What You’ll Do
\n\n
Serve as a coordinator for assigned vaccine clinical trials, supporting study activities from start-up through closeout as needed
\nExecute participant visit flow independently, including visit preparation, patient interaction, protocol-related procedures, data collection, and documentation
\nSupport high-volume clinic days by helping maintain efficient visit flow, clear communication, and accurate completion of study-required tasks
\nLead patient interactions with clarity and compassion, ensuring participants feel informed and supported throughout their study experience
\nPerform clinical procedures as required by protocol, which may include vital signs, EKGs, phlebotomy, specimen collection, specimen processing, and other study-specific assessments
\nMaintain accurate, timely, audit-ready documentation across source documents, CRFs, EDC systems, CTMS platforms, and other study tools
\nTrack, document, and escalate adverse events, deviations, safety findings, and protocol-related issues in accordance with study and regulatory requirements
\nCommunicate directly and professionally with investigators, sponsors, CROs, monitors, vendors, and internal team members
\nSupport site readiness for monitoring visits, sponsor communications, internal quality review, and audits
\nFollow study protocols, SOPs, Good Clinical Practice, Good Documentation Practices, and infection control expectations to support compliant, high-quality trial execution
\nHelp maintain organized study materials, lab workflows, visit supplies, and documentation needed for efficient site operations
\nContribute to a fast-paced, team-based environment where quality, urgency, patient experience, and data integrity all matter
\n\n
What We’re Looking For
\nYou have clinical research experience and are ready to operate with more ownership. You’re organized, detail-oriented, comfortable managing competing priorities, and able to follow through without heavy oversight.
\n\n
Essential Qualifications
\nBachelor’s degree with 1+ year of relevant experience, OR Associate’s degree with 3+ years of relevant experience, OR High school diploma with 4+ years of relevant experience and at least 1 year of CRC experience
\nPrior experience in clinical research, including exposure to clinical trial coordination, study visits, source documentation, and protocol-driven workflows
\nExperience performing or supporting clinical procedures, which may include vital signs, EKGs, phlebotomy, specimen collection, specimen processing, or lab-related workflows
\nComfortable working independently in a fast-paced, site-based clinical research environment
\nAbility to support high-volume patient visits while maintaining accuracy, professionalism, and a patient-centered approach
\nStrong documentation skills and understanding of audit-ready clinical research standards
\nFamiliarity with EDC platforms, clinical trial management systems, eSource tools, EMRs, lab portals, or other clinical documentation systems
\nWorking knowledge of Good Clinical Practice, Good Documentation Practices, protocol adherence, and regulatory expectations
\nStrong communication skills with the ability to interact professionally with patients, caregivers, investigators, site staff, sponsors, CROs, monitors, and internal teams
\nAbility to maintain professionalism, confidentiality, and care when working with patients and sensitive information
\n\n
Preferred Qualifications
\nExperience supporting vaccine studies, infectious disease studies, immunization clinics, urgent care, primary care, or other high-volume patient-facing clinical environments
\nPrior experience serving as a primary or lead coordinator for assigned studies
\nExperience with adverse event documentation, protocol deviations, query resolution, monitoring visits, and sponsor/CRO communication
\nActive or prior ICH-GCP, IATA, phlebotomy, or related clinical research certifications
\nExperience supporting start-up, closeout, or audit/monitoring readiness activities
\nComfort adapting quickly to study-specific workflows, systems, and enrollment timelines
\n\n
Engagement Details
\nThis is a 1099 independent contractor opportunity designed to support current high-volume vaccine study needs while giving the right person a chance to learn, contribute quickly, demonstrate ownership, and be considered for future opportunities. For contractors who perform well and align with business needs, there may be an opportunity to be considered for full-time employment over time.
\nPhysical Requirements & Work Environment
\nThis role is performed on-site at a clinical or office facility and requires prolonged periods of sitting, standing, or walking throughout the work environment
\nRequires the ability to communicate clearly in verbal and written forms and to read and interpret detailed materials
\nMust be able to navigate a clinical facility, including areas with limited space, and transport supplies or work materials as needed
\nMay be required to wear personal protective equipment (PPE) in accordance with facility protocols
\nTravel between company sites, meetings, or partner locations may be required
\nReasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the role
\n\n
Why Join Profound Research?
\nMeaningful Impact: Every role at Profound contributes to advancing medical knowledge and expanding therapeutic options for patients – the work we do here matters
\nProfessional Growth: We invest in our people through comprehensive training, certification support, and ongoing education to help you grow in your role and your career
\nLeadership & Advancement: Profound is a place where initiative is recognized. We actively support internal growth and create pathways for people to take on greater responsibility over time
\nCollaborative Culture: You’ll work alongside a team of dedicated professionals who are passionate about clinical research and committed to doing it well
\nFull Benefits Package: Competitive compensation, health insurance, PTO, retirement plan, and professional development support
\nDiverse Clinical Exposure: Work across multiple therapeutic areas and study phases, building a breadth of experience that’s rare in a single organization (for Clinical / Patient-Facing roles)
\nWhy This Role Exists
\nIf you’re ready to bring your clinical research experience into a fast-paced, high-volume environment, this role offers an opportunity to make an immediate impact.
\n\n
As a Clinical Research Coordinator I at Profound Research, you’ll support the execution of high-volume vaccine clinical trials at one of our sites. You’ll help manage study activities, lead participant visits, complete protocol-required procedures and documentation, and work closely with investigators, sponsors, CROs, and internal teams. This is not an entry-level support role – you’ll be expected to operate with ownership, sound judgment, and a strong understanding of clinical research standards.
\n\n
This is a 1099 contract opportunity designed to support near-term vaccine study needs, with the potential to convert to a full-time position based on business needs, performance, and role availability. If you’re looking to build on your clinical research experience with a growing organization that values accountability, quality, and patient-centered execution, we’d like to hear from you.
\n\n
What You’ll Do
\n\n
Serve as a coordinator for assigned vaccine clinical trials, supporting study activities from start-up through closeout as needed
\nExecute participant visit flow independently, including visit preparation, patient interaction, protocol-related procedures, data collection, and documentation
\nSupport high-volume clinic days by helping maintain efficient visit flow, clear communication, and accurate completion of study-required tasks
\nLead patient interactions with clarity and compassion, ensuring participants feel informed and supported throughout their study experience
\nPerform clinical procedures as required by protocol, which may include vital signs, EKGs, phlebotomy, specimen collection, specimen processing, and other study-specific assessments
\nMaintain accurate, timely, audit-ready documentation across source documents, CRFs, EDC systems, CTMS platforms, and other study tools
\nTrack, document, and escalate adverse events, deviations, safety findings, and protocol-related issues in accordance with study and regulatory requirements
\nCommunicate directly and professionally with investigators, sponsors, CROs, monitors, vendors, and internal team members
\nSupport site readiness for monitoring visits, sponsor communications, internal quality review, and audits
\nFollow study protocols, SOPs, Good Clinical Practice, Good Documentation Practices, and infection control expectations to support compliant, high-quality trial execution
\nHelp maintain organized study materials, lab workflows, visit supplies, and documentation needed for efficient site operations
\nContribute to a fast-paced, team-based environment where quality, urgency, patient experience, and data integrity all matter
\n\n
What We’re Looking For
\nYou have clinical research experience and are ready to operate with more ownership. You’re organized, detail-oriented, comfortable managing competing priorities, and able to follow through without heavy oversight.
\n\n
Essential Qualifications
\nBachelor’s degree with 1+ year of relevant experience, OR Associate’s degree with 3+ years of relevant experience, OR High school diploma with 4+ years of relevant experience and at least 1 year of CRC experience
\nPrior experience in clinical research, including exposure to clinical trial coordination, study visits, source documentation, and protocol-driven workflows
\nExperience performing or supporting clinical procedures, which may include vital signs, EKGs, phlebotomy, specimen collection, specimen processing, or lab-related workflows
\nComfortable working independently in a fast-paced, site-based clinical research environment
\nAbility to support high-volume patient visits while maintaining accuracy, professionalism, and a patient-centered approach
\nStrong documentation skills and understanding of audit-ready clinical research standards
\nFamiliarity with EDC platforms, clinical trial management systems, eSource tools, EMRs, lab portals, or other clinical documentation systems
\nWorking knowledge of Good Clinical Practice, Good Documentation Practices, protocol adherence, and regulatory expectations
\nStrong communication skills with the ability to interact professionally with patients, caregivers, investigators, site staff, sponsors, CROs, monitors, and internal teams
\nAbility to maintain professionalism, confidentiality, and care when working with patients and sensitive information
\n\n
Preferred Qualifications
\nExperience supporting vaccine studies, infectious disease studies, immunization clinics, urgent care, primary care, or other high-volume patient-facing clinical environments
\nPrior experience serving as a primary or lead coordinator for assigned studies
\nExperience with adverse event documentation, protocol deviations, query resolution, monitoring visits, and sponsor/CRO communication
\nActive or prior ICH-GCP, IATA, phlebotomy, or related clinical research certifications
\nExperience supporting start-up, closeout, or audit/monitoring readiness activities
\nComfort adapting quickly to study-specific workflows, systems, and enrollment timelines
\n\n
Engagement Details
\nThis is a 1099 independent contractor opportunity designed to support current high-volume vaccine study needs while giving the right person a chance to learn, contribute quickly, demonstrate ownership, and be considered for future opportunities. For contractors who perform well and align with business needs, there may be an opportunity to be considered for full-time employment over time.
\nWhy This Role Exists
\nIf you’re ready to bring your clinical research experience into a fast-paced, high-volume environment, this role offers an opportunity to make an immediate impact.
\n\n
As a Clinical Research Coordinator I at Profound Research, you’ll support the execution of high-volume vaccine clinical trials at one of our sites. You’ll help manage study activities, lead participant visits, complete protocol-required procedures and documentation, and work closely with investigators, sponsors, CROs, and internal teams. This is not an entry-level support role – you’ll be expected to operate with ownership, sound judgment, and a strong understanding of clinical research standards.
\n\n
This is a 1099 contract opportunity designed to support near-term vaccine study needs, with the potential to convert to a full-time position based on business needs, performance, and role availability. If you’re looking to build on your clinical research experience with a growing organization that values accountability, quality, and patient-centered execution, we’d like to hear from you.
\n\n
What You’ll Do
\n\n
Serve as a coordinator for assigned vaccine clinical trials, supporting study activities from start-up through closeout as needed
\nExecute participant visit flow independently, including visit preparation, patient interaction, protocol-related procedures, data collection, and documentation
\nSupport high-volume clinic days by helping maintain efficient visit flow, clear communication, and accurate completion of study-required tasks
\nLead patient interactions with clarity and compassion, ensuring participants feel informed and supported throughout their study experience
\nPerform clinical procedures as required by protocol, which may include vital signs, EKGs, phlebotomy, specimen collection, specimen processing, and other study-specific assessments
\nMaintain accurate, timely, audit-ready documentation across source documents, CRFs, EDC systems, CTMS platforms, and other study tools
\nTrack, document, and escalate adverse events, deviations, safety findings, and protocol-related issues in accordance with study and regulatory requirements
\nCommunicate directly and professionally with investigators, sponsors, CROs, monitors, vendors, and internal team members
\nSupport site readiness for monitoring visits, sponsor communications, internal quality review, and audits
\nFollow study protocols, SOPs, Good Clinical Practice, Good Documentation Practices, and infection control expectations to support compliant, high-quality trial execution
\nHelp maintain organized study materials, lab workflows, visit supplies, and documentation needed for efficient site operations
\nContribute to a fast-paced, team-based environment where quality, urgency, patient experience, and data integrity all matter
\n\n
What We’re Looking For
\nYou have clinical research experience and are ready to operate with more ownership. You’re organized, detail-oriented, comfortable managing competing priorities, and able to follow through without heavy oversight.
\n\n
Essential Qualifications
\nBachelor’s degree with 1+ year of relevant experience, OR Associate’s degree with 3+ years of relevant experience, OR High school diploma with 4+ years of relevant experience and at least 1 year of CRC experience
\nPrior experience in clinical research, including exposure to clinical trial coordination, study visits, source documentation, and protocol-driven workflows
\nExperience performing or supporting clinical procedures, which may include vital signs, EKGs, phlebotomy, specimen collection, specimen processing, or lab-related workflows
\nComfortable working independently in a fast-paced, site-based clinical research environment
\nAbility to support high-volume patient visits while maintaining accuracy, professionalism, and a patient-centered approach
\nStrong documentation skills and understanding of audit-ready clinical research standards
\nFamiliarity with EDC platforms, clinical trial management systems, eSource tools, EMRs, lab portals, or other clinical documentation systems
\nWorking knowledge of Good Clinical Practice, Good Documentation Practices, protocol adherence, and regulatory expectations
\nStrong communication skills with the ability to interact professionally with patients, caregivers, investigators, site staff, sponsors, CROs, monitors, and internal teams
\nAbility to maintain professionalism, confidentiality, and care when working with patients and sensitive information
\n\n
Preferred Qualifications
\nExperience supporting vaccine studies, infectious disease studies, immunization clinics, urgent care, primary care, or other high-volume patient-facing clinical environments
\nPrior experience serving as a primary or lead coordinator for assigned studies
\nExperience with adverse event documentation, protocol deviations, query resolution, monitoring visits, and sponsor/CRO communication
\nActive or prior ICH-GCP, IATA, phlebotomy, or related clinical research certifications
\nExperience supporting start-up, closeout, or audit/monitoring readiness activities
\nComfort adapting quickly to study-specific workflows, systems, and enrollment timelines
\n\n
Engagement Details
\nThis is a 1099 independent contractor opportunity designed to support current high-volume vaccine study needs while giving the right person a chance to learn, contribute quickly, demonstrate ownership, and be considered for future opportunities. For contractors who perform well and align with business needs, there may be an opportunity to be considered for full-time employment over time.
\nAbout Profound Research
\nProfound Research partners with community physicians to offer clinical trials as a therapeutic option for their patients. We handle all infrastructure, regulatory compliance, and administrative operations so physicians can focus on patient care. Our model gives patients access to the newest therapies while maintaining the trusted patient-physician relationship.
\n\n
Our Mission: Improving lives by providing advanced therapeutic options
\n\n
Our Vision: Creating the absolute best patient-physician experience in clinical research
\n\n
Our Values:
\nCompassion: We prioritize the patient-physician relationship, ensuring every interaction is service-oriented and patient-centered
\nUrgency: We work hard and practice selflessness, acting swiftly and decisively to meet the needs of our patients, partners, and colleagues
\nSolution Orientation: We embrace challenges with a positive mindset, communicate directly, and identify and implement effective solutions with efficiency
\nExcellence: We insist on excellence, holding ourselves accountable and empowering each other to deliver best-in-class service while maintaining the highest ethical and scientific standards
\nWhy This Role Exists
\nAt Profound Research, patient recruitment is essential to expanding access to clinical trials and helping studies enroll the right participants with speed, care, and quality.
\n\n
The Patient Recruitment Specialist will provide remote, centralized recruitment support for high-volume vaccine/flu clinical trials. This role will focus primarily on patient outreach, inbound lead follow-up, phone pre-screening, scheduling, and accurate documentation across recruitment systems. As one of the first points of contact for prospective participants, this person will help create a responsive, compassionate, and well-organized recruitment experience that supports both enrollment goals and patient trust.
\n\n
This is a 1099 contract opportunity designed to support near-term study enrollment needs, with the potential to convert to a full-time position based on business needs, performance, and role availability. Whether you’re looking to build on prior clinical research experience or take the next step into the field, this is an opportunity to contribute to meaningful work with a growing organization that values strong communication, follow-through, and patient-centered service.
\n\n
What You’ll Do
\n\n
Conduct high-volume outbound outreach to prospective clinical trial participants who may be interested in vaccine/flu studies
\nRespond to inbound patient inquiries and recruitment leads in a timely, professional, and patient-centered manner
\nServe as an early point of contact for prospective participants, creating a supportive experience grounded in empathy, clarity, and excellent customer service
\nPre-screen potential participants by reviewing study-specific eligibility criteria and documenting responses accurately
\nSchedule qualified participants for screening visits and coordinate next steps with the appropriate site or study team
\nSupport patient follow-up to help improve show rates, maintain engagement, and reduce barriers to participation
\nMaintain accurate, timely records across CTMS, scheduling tools, screening logs, and third-party recruitment platforms
\nTrack outreach activity, patient responses, scheduling status, and other recruitment metrics as requested
\nApply working knowledge of Good Clinical Practice (GDP), FDA regulations, study protocols, and internal policies across patient interactions and documentation
\nCommunicate clearly with recruitment leadership, site teams, study coordinators, and support staff regarding patient status, recruitment progress, and potential issues
\nContribute to a fast-moving, high-volume recruitment environment with urgency, professionalism, and attention to detail
\nAssist in obtaining medical records to confirm eligibility for potential research participants
\n\n
What You’ll Bring
\n\n
Essential Qualifications
\nExperience in patient recruitment, call center operations, clinical research support, healthcare customer service, sales, or another high-volume outreach environment
\nStrong professional phone presence and ability to build trust quickly with prospective participants
\nComfort conducting both inbound and outbound patient communication
\nAbility to communicate with empathy, patience, and clarity while maintaining study-specific accuracy
\nStrong attention to detail and comfort documenting information across multiple systems
\nComfort with medical terminology and protocol-driven eligibility questions
\nTechnical aptitude, including experience using databases, scheduling tools, spreadsheets, CTMS platforms, or patient tracking systems
\nResults-oriented mindset with the ability to support enrollment goals while maintaining a high-quality patient experience
\nAbility to work independently in a remote environment while maintaining strong communication with the broader recruitment team
\n\n
Preferred Qualifications
\nPrior clinical research experience, especially in patient recruitment or patient engagement
\nExperience supporting vaccine, infectious disease, or high-enrollment clinical trials
\nFamiliarity with Good Clinical Practice and FDA-regulated research environments
\nExperience using CTMS platforms, patient recruitment platforms, or third-party lead management tools
\nAssociate’s degree or higher
\nCNA, medical assistant, or other healthcare-related background
\n\n
Engagement Details
\nThis is a 1099 independent contractor opportunity supporting high-volume vaccine/flu trial recruitment. Contract duration and weekly workload may vary based on study needs, enrollment timelines, and business requirements. This opportunity may lead to consideration for a full-time position, but conversion is not guaranteed.
\nAbout Profound Research
\nProfound Research partners with community physicians to offer clinical trials as a therapeutic option for their patients. We handle all infrastructure, regulatory compliance, and administrative operations so physicians can focus on patient care. Our model gives patients access to the newest therapies while maintaining the trusted patient-physician relationship.
\n\n
Our Mission: Improving lives by providing advanced therapeutic options
\n\n
Our Vision: Creating the absolute best patient-physician experience in clinical research
\n\n
Our Values:
\nCompassion: We prioritize the patient-physician relationship, ensuring every interaction is service-oriented and patient-centered
\nUrgency: We work hard and practice selflessness, acting swiftly and decisively to meet the needs of our patients, partners, and colleagues
\nSolution Orientation: We embrace challenges with a positive mindset, communicate directly, and identify and implement effective solutions with efficiency
\nExcellence: We insist on excellence, holding ourselves accountable and empowering each other to deliver best-in-class service while maintaining the highest ethical and scientific standards
\nWhy This Role Exists
\nAt Profound Research, patient recruitment is essential to expanding access to clinical trials and helping studies enroll the right participants with speed, care, and quality.
\n\n
The Patient Recruitment Specialist will provide remote, centralized recruitment support for high-volume vaccine/flu clinical trials. This role will focus primarily on patient outreach, inbound lead follow-up, phone pre-screening, scheduling, and accurate documentation across recruitment systems. As one of the first points of contact for prospective participants, this person will help create a responsive, compassionate, and well-organized recruitment experience that supports both enrollment goals and patient trust.
\n\n
This is a 1099 contract opportunity designed to support near-term study enrollment needs, with the potential to convert to a full-time position based on business needs, performance, and role availability. Whether you’re looking to build on prior clinical research experience or take the next step into the field, this is an opportunity to contribute to meaningful work with a growing organization that values strong communication, follow-through, and patient-centered service.
\n\n
What You’ll Do
\n\n
Conduct high-volume outbound outreach to prospective clinical trial participants who may be interested in vaccine/flu studies
\nRespond to inbound patient inquiries and recruitment leads in a timely, professional, and patient-centered manner
\nServe as an early point of contact for prospective participants, creating a supportive experience grounded in empathy, clarity, and excellent customer service
\nPre-screen potential participants by reviewing study-specific eligibility criteria and documenting responses accurately
\nSchedule qualified participants for screening visits and coordinate next steps with the appropriate site or study team
\nSupport patient follow-up to help improve show rates, maintain engagement, and reduce barriers to participation
\nMaintain accurate, timely records across CTMS, scheduling tools, screening logs, and third-party recruitment platforms
\nTrack outreach activity, patient responses, scheduling status, and other recruitment metrics as requested
\nApply working knowledge of Good Clinical Practice (GDP), FDA regulations, study protocols, and internal policies across patient interactions and documentation
\nCommunicate clearly with recruitment leadership, site teams, study coordinators, and support staff regarding patient status, recruitment progress, and potential issues
\nContribute to a fast-moving, high-volume recruitment environment with urgency, professionalism, and attention to detail
\nAssist in obtaining medical records to confirm eligibility for potential research participants
\n\n
What You’ll Bring
\n\n
Essential Qualifications
\nExperience in patient recruitment, call center operations, clinical research support, healthcare customer service, sales, or another high-volume outreach environment
\nStrong professional phone presence and ability to build trust quickly with prospective participants
\nComfort conducting both inbound and outbound patient communication
\nAbility to communicate with empathy, patience, and clarity while maintaining study-specific accuracy
\nStrong attention to detail and comfort documenting information across multiple systems
\nComfort with medical terminology and protocol-driven eligibility questions
\nTechnical aptitude, including experience using databases, scheduling tools, spreadsheets, CTMS platforms, or patient tracking systems
\nResults-oriented mindset with the ability to support enrollment goals while maintaining a high-quality patient experience
\nAbility to work independently in a remote environment while maintaining strong communication with the broader recruitment team
\n\n
Preferred Qualifications
\nPrior clinical research experience, especially in patient recruitment or patient engagement
\nExperience supporting vaccine, infectious disease, or high-enrollment clinical trials
\nFamiliarity with Good Clinical Practice and FDA-regulated research environments
\nExperience using CTMS platforms, patient recruitment platforms, or third-party lead management tools
\nAssociate’s degree or higher
\nCNA, medical assistant, or other healthcare-related background
\n\n
Engagement Details
\nThis is a 1099 independent contractor opportunity supporting high-volume vaccine/flu trial recruitment. Contract duration and weekly workload may vary based on study needs, enrollment timelines, and business requirements. This opportunity may lead to consideration for a full-time position, but conversion is not guaranteed.
\nPhysical Requirements & Work Environment
\nThis role is performed on-site at a clinical or office facility and requires prolonged periods of sitting, standing, or walking throughout the work environment
\nRequires the ability to communicate clearly in verbal and written forms and to read and interpret detailed materials
\nMust be able to navigate a clinical facility, including areas with limited space, and transport supplies or work materials as needed
\nMay be required to wear personal protective equipment (PPE) in accordance with facility protocols
\nTravel between company sites, meetings, or partner locations may be required
\nReasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the role
\n\n
Why Join Profound Research?
\nMeaningful Impact: Every role at Profound contributes to advancing medical knowledge and expanding therapeutic options for patients – the work we do here matters
\nProfessional Growth: We invest in our people through comprehensive training, certification support, and ongoing education to help you grow in your role and your career
\nLeadership & Advancement: Profound is a place where initiative is recognized. We actively support internal growth and create pathways for people to take on greater responsibility over time
\nCollaborative Culture: You’ll work alongside a team of dedicated professionals who are passionate about clinical research and committed to doing it well
\nFull Benefits Package: Competitive compensation, health insurance, PTO, retirement plan, and professional development support
\nDiverse Clinical Exposure: Work across multiple therapeutic areas and study phases, building a breadth of experience that’s rare in a single organization (for Clinical / Patient-Facing roles)
\nWhy This Role Exists
\nAt Profound Research, patient engagement is central to delivering high-quality clinical trials and expanding access to advanced therapeutic options.
\n\n
The Embedded Patient Engagement Specialist owns an onsite recruitment and patient engagement presence that accelerates enrollment and improves the patient experience. This role drives full-cycle patient recruitment – from working inbound leads and physician referrals, through EMR and chart review, phone pre-screening and visit scheduling, to helping patients navigate the screening process and supporting show rates through randomization.
\n\n
Building strong relationships with physicians and site staff and partnering closely with Clinical Research Coordinators (CRCs), the Embedded Patient Engagement Specialist helps remove barriers to participation, strengthen referral pipelines, and support timely, high-quality trial execution. This position is embedded in a clinical trial site, may support additional sites as needed, and reports to an offsite Manager, Patient Recruitment.
\n\n
What You’ll Do
\n\n
Serve as the on-site face of Profound Research, building relationships with investigators and site staff and maintaining a consistent on-site presence to keep recruitment aligned with study goals
\nOwn the full recruitment cycle for assigned studies – from chart review and patient outreach through pre-screening, visit scheduling, and follow-up through randomization
\nBe the first point of contact for prospective participants, delivering a patient-centered experience that drives both enrollment and retention
\nRespond to inbound inquiries within 24-48 hours and conduct appropriate pre-screening assessments in line with study protocols and inclusion/exclusion criteria
\nAttend Pre-Site Visits (PSVs), Site Initiation Visits (SIVs), and physician meetings to contribute to study-specific recruitment planning and share performance updates with investigators and internal stakeholders
\nMaintain accurate, timely records across CTMS, scheduling tools, screening logs, and third-party recruitment platforms
\nApply working knowledge of GCP, FDA regulations, and internal policies across all patient interactions and documentation
\nRepresent Profound Research at occasional community events and health fairs, and support expansion of the patient database across therapeutic areas
\nShare best practices across sites and actively contribute to improving recruitment capabilities over time
\n\n
Requirements
\nEssential Qualifications
\nStrong ability to build relationships with investigators, site staff, and patients
\nHigh level of comfort in high-volume outreach environments, both inbound and outbound
\nStrong communication skills and professional phone presence with a patient-first mindset
\nProficiency in medical terminology across multiple therapeutic areas
\nStrong technical aptitude, including experience with CTMS and patient tracking systems
\nResults-oriented mindset with the ability to manage competing priorities and meet enrollment goals
\n\n
Preferred Qualifications
\nAssociate’s degree or higher
\nExperience in a call center, sales, or performance-driven environment
\nExperience supporting multi-site clinical research operations
\nDemonstrated experience driving patient recruitment and engagement in a clinical research setting
\n\n
\n
Why This Role Exists
\nAt Profound Research, patient engagement is central to delivering high-quality clinical trials and expanding access to advanced therapeutic options.
\n\n
The Embedded Patient Engagement Specialist owns an onsite recruitment and patient engagement presence that accelerates enrollment and improves the patient experience. This role drives full-cycle patient recruitment – from working inbound leads and physician referrals, through EMR and chart review, phone pre-screening and visit scheduling, to helping patients navigate the screening process and supporting show rates through randomization.
\n\n
Building strong relationships with physicians and site staff and partnering closely with Clinical Research Coordinators (CRCs), the Embedded Patient Engagement Specialist helps remove barriers to participation, strengthen referral pipelines, and support timely, high-quality trial execution. This position is embedded in a clinical trial site, may support additional sites as needed, and reports to an offsite Manager, Patient Recruitment.
\n\n
What You’ll Do
\n\n
Serve as the on-site face of Profound Research, building relationships with investigators and site staff and maintaining a consistent on-site presence to keep recruitment aligned with study goals
\nOwn the full recruitment cycle for assigned studies – from chart review and patient outreach through pre-screening, visit scheduling, and follow-up through randomization
\nBe the first point of contact for prospective participants, delivering a patient-centered experience that drives both enrollment and retention
\nRespond to inbound inquiries within 24-48 hours and conduct appropriate pre-screening assessments in line with study protocols and inclusion/exclusion criteria
\nAttend Pre-Site Visits (PSVs), Site Initiation Visits (SIVs), and physician meetings to contribute to study-specific recruitment planning and share performance updates with investigators and internal stakeholders
\nMaintain accurate, timely records across CTMS, scheduling tools, screening logs, and third-party recruitment platforms
\nApply working knowledge of GCP, FDA regulations, and internal policies across all patient interactions and documentation
\nRepresent Profound Research at occasional community events and health fairs, and support expansion of the patient database across therapeutic areas
\nShare best practices across sites and actively contribute to improving recruitment capabilities over time
\n\n
Requirements
\nEssential Qualifications
\nStrong ability to build relationships with investigators, site staff, and patients
\nHigh level of comfort in high-volume outreach environments, both inbound and outbound
\nStrong communication skills and professional phone presence with a patient-first mindset
\nProficiency in medical terminology across multiple therapeutic areas
\nStrong technical aptitude, including experience with CTMS and patient tracking systems
\nResults-oriented mindset with the ability to manage competing priorities and meet enrollment goals
\n\n
Preferred Qualifications
\nAssociate’s degree or higher
\nExperience in a call center, sales, or performance-driven environment
\nExperience supporting multi-site clinical research operations
\nDemonstrated experience driving patient recruitment and engagement in a clinical research setting
\n\n
\n
Physical Requirements & Work Environment
\nThis role is performed on-site at a clinical or office facility and requires prolonged periods of sitting, standing, or walking throughout the work environment
\nRequires the ability to communicate clearly in verbal and written forms and to read and interpret detailed materials
\nMust be able to navigate a clinical facility, including areas with limited space, and transport supplies or work materials as needed
\nMay be required to wear personal protective equipment (PPE) in accordance with facility protocols
\nTravel between company sites, meetings, or partner locations may be required
\nReasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the role
\n\n
Why Join Profound Research?
\nMeaningful Impact: Every role at Profound contributes to advancing medical knowledge and expanding therapeutic options for patients – the work we do here matters
\nProfessional Growth: We invest in our people through comprehensive training, certification support, and ongoing education to help you grow in your role and your career
\nLeadership & Advancement: Profound is a place where initiative is recognized. We actively support internal growth and create pathways for people to take on greater responsibility over time
\nCollaborative Culture: You’ll work alongside a team of dedicated professionals who are passionate about clinical research and committed to doing it well
\nFull Benefits Package: Competitive compensation, health insurance, PTO, retirement plan, and professional development support
\nDiverse Clinical Exposure: Work across multiple therapeutic areas and study phases, building a breadth of experience that’s rare in a single organization (for Clinical / Patient-Facing roles)
\nWhy This Role Exists
\nAt Profound Research, patient engagement is central to delivering high-quality clinical trials and expanding access to advanced therapeutic options.
\n\n
The Embedded Patient Engagement Specialist owns an onsite recruitment and patient engagement presence that accelerates enrollment and improves the patient experience. This role drives full-cycle patient recruitment – from working inbound leads and physician referrals, through EMR and chart review, phone pre-screening and visit scheduling, to helping patients navigate the screening process and supporting show rates through randomization.
\n\n
Building strong relationships with physicians and site staff and partnering closely with Clinical Research Coordinators (CRCs), the Embedded Patient Engagement Specialist helps remove barriers to participation, strengthen referral pipelines, and support timely, high-quality trial execution. This position is embedded in a clinical trial site, may support additional sites as needed, and reports to an offsite Manager, Patient Recruitment.
\n\n
What You’ll Do
\n\n
Serve as the on-site face of Profound Research, building relationships with investigators and site staff and maintaining a consistent on-site presence to keep recruitment aligned with study goals
\nOwn the full recruitment cycle for assigned studies – from chart review and patient outreach through pre-screening, visit scheduling, and follow-up through randomization
\nBe the first point of contact for prospective participants, delivering a patient-centered experience that drives both enrollment and retention
\nRespond to inbound inquiries within 24-48 hours and conduct appropriate pre-screening assessments in line with study protocols and inclusion/exclusion criteria
\nAttend Pre-Site Visits (PSVs), Site Initiation Visits (SIVs), and physician meetings to contribute to study-specific recruitment planning and share performance updates with investigators and internal stakeholders
\nMaintain accurate, timely records across CTMS, scheduling tools, screening logs, and third-party recruitment platforms
\nApply working knowledge of GCP, FDA regulations, and internal policies across all patient interactions and documentation
\nRepresent Profound Research at occasional community events and health fairs, and support expansion of the patient database across therapeutic areas
\nShare best practices across sites and actively contribute to improving recruitment capabilities over time
\n\n
Requirements
\nEssential Qualifications
\nStrong ability to build relationships with investigators, site staff, and patients
\nHigh level of comfort in high-volume outreach environments, both inbound and outbound
\nStrong communication skills and professional phone presence with a patient-first mindset
\nProficiency in medical terminology across multiple therapeutic areas
\nStrong technical aptitude, including experience with CTMS and patient tracking systems
\nResults-oriented mindset with the ability to manage competing priorities and meet enrollment goals
\n\n
Preferred Qualifications
\nAssociate’s degree or higher
\nExperience in a call center, sales, or performance-driven environment
\nExperience supporting multi-site clinical research operations
\nDemonstrated experience driving patient recruitment and engagement in a clinical research setting
\n\n
\n
\n
Why This Role Exists
\nAt Profound Research, patient engagement is central to delivering high-quality clinical trials and expanding access to advanced therapeutic options.
\n\n
The Embedded Patient Engagement Specialist owns an onsite recruitment and patient engagement presence that accelerates enrollment and improves the patient experience. This role drives full-cycle patient recruitment – from working inbound leads and physician referrals, through EMR and chart review, phone pre-screening and visit scheduling, to helping patients navigate the screening process and supporting show rates through randomization.
\n\n
Building strong relationships with physicians and site staff and partnering closely with Clinical Research Coordinators (CRCs), the Embedded Patient Engagement Specialist helps remove barriers to participation, strengthen referral pipelines, and support timely, high-quality trial execution. This position is embedded in a clinical trial site, may support additional sites as needed, and reports to an offsite Manager, Patient Recruitment.
\n\n
What You’ll Do
\n\n
Serve as the on-site face of Profound Research, building relationships with investigators and site staff and maintaining a consistent on-site presence to keep recruitment aligned with study goals
\nOwn the full recruitment cycle for assigned studies – from chart review and patient outreach through pre-screening, visit scheduling, and follow-up through randomization
\nBe the first point of contact for prospective participants, delivering a patient-centered experience that drives both enrollment and retention
\nRespond to inbound inquiries within 24-48 hours and conduct appropriate pre-screening assessments in line with study protocols and inclusion/exclusion criteria
\nAttend Pre-Site Visits (PSVs), Site Initiation Visits (SIVs), and physician meetings to contribute to study-specific recruitment planning and share performance updates with investigators and internal stakeholders
\nMaintain accurate, timely records across CTMS, scheduling tools, screening logs, and third-party recruitment platforms
\nApply working knowledge of GCP, FDA regulations, and internal policies across all patient interactions and documentation
\nRepresent Profound Research at occasional community events and health fairs, and support expansion of the patient database across therapeutic areas
\nShare best practices across sites and actively contribute to improving recruitment capabilities over time
\n\n
Requirements
\nEssential Qualifications
\nStrong ability to build relationships with investigators, site staff, and patients
\nHigh level of comfort in high-volume outreach environments, both inbound and outbound
\nStrong communication skills and professional phone presence with a patient-first mindset
\nProficiency in medical terminology across multiple therapeutic areas
\nStrong technical aptitude, including experience with CTMS and patient tracking systems
\nResults-oriented mindset with the ability to manage competing priorities and meet enrollment goals
\n\n
Preferred Qualifications
\nAssociate’s degree or higher
\nExperience in a call center, sales, or performance-driven environment
\nExperience supporting multi-site clinical research operations
\nDemonstrated experience driving patient recruitment and engagement in a clinical research setting
\n\n
\n
\n
Physical Requirements & Work Environment
\nThis role is performed on-site at a clinical or office facility and requires prolonged periods of sitting, standing, or walking throughout the work environment
\nRequires the ability to communicate clearly in verbal and written forms and to read and interpret detailed materials
\nMust be able to navigate a clinical facility, including areas with limited space, and transport supplies or work materials as needed
\nMay be required to wear personal protective equipment (PPE) in accordance with facility protocols
\nTravel between company sites, meetings, or partner locations may be required
\nReasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the role
\n\n
Why Join Profound Research?
\nMeaningful Impact: Every role at Profound contributes to advancing medical knowledge and expanding therapeutic options for patients – the work we do here matters
\nProfessional Growth: We invest in our people through comprehensive training, certification support, and ongoing education to help you grow in your role and your career
\nLeadership & Advancement: Profound is a place where initiative is recognized. We actively support internal growth and create pathways for people to take on greater responsibility over time
\nCollaborative Culture: You’ll work alongside a team of dedicated professionals who are passionate about clinical research and committed to doing it well
\nFull Benefits Package: Competitive compensation, health insurance, PTO, retirement plan, and professional development support
\nDiverse Clinical Exposure: Work across multiple therapeutic areas and study phases, building a breadth of experience that’s rare in a single organization (for Clinical / Patient-Facing roles)
\nStart Your Career in Clinical Research
\nIf you’re curious about how new treatments reach patients, detail-oriented by nature, and energized by work that genuinely matters – this is where that career begins.
\n\n
As an Assistant Clinical Research Coordinator at Profound Research, you’ll work alongside experienced clinical research staff at one of our sites, supporting the day-to-day execution of clinical trials that give patients access to therapies they couldn’t otherwise reach. You’ll learn by doing – gaining hands-on experience in study coordination, patient interaction, data collection, and clinical procedures – with a clear path to grow into greater ownership and responsibility over time.
\n\n
This isn’t a behind-the-desk role. You’ll be present with patients, part of a team, and contributing to research that has real-world impact from day one.
\n\n
What You’ll Do
\n\n
Support the coordination of active clinical trials, including patient visits, scheduling, and study-related procedures
\nAssist with data collection and documentation, learning to apply the rigorous standards that clinical research demands
\nPerform and develop competency in clinical procedures including vital signs, EKGs, phlebotomy, and specimen processing
\nInteract directly with study participants – greeting them, explaining visit steps, and ensuring they feel supported throughout the process
\nWork closely with Clinical Research Coordinators and site leadership, asking questions, seeking feedback, and building your clinical knowledge base
\nContribute to a compliant, audit-ready site by following established protocols, SOPs, and Good Documentation Practices
\n\n
What We’re Looking For
\nYou don’t need to have done this exact job before. You need to be the kind of person who takes ownership of their work, communicates clearly, pays close attention to detail, and genuinely cares about the patient experience. The rest we’ll help you build.
\n\n
High school diploma or technical degree with 3+ years of relevant experience in life sciences, OR Associate’s degree with 1+ year of relevant experience, OR Bachelor’s degree with relevant coursework or experience in a clinical or life sciences setting
\nFamiliarity with medical terminology and basic clinical procedures is a plus
\nComfortable working in a fast-paced, team-based environment
\nProficient with standard computer tools; able to learn new systems quickly
\nICH-GCP and IATA certification required within a defined timeframe upon hire (we’ll support you through it)
\nStart Your Career in Clinical Research
\nIf you’re curious about how new treatments reach patients, detail-oriented by nature, and energized by work that genuinely matters – this is where that career begins.
\n\n
As an Assistant Clinical Research Coordinator at Profound Research, you’ll work alongside experienced clinical research staff at one of our sites, supporting the day-to-day execution of clinical trials that give patients access to therapies they couldn’t otherwise reach. You’ll learn by doing – gaining hands-on experience in study coordination, patient interaction, data collection, and clinical procedures – with a clear path to grow into greater ownership and responsibility over time.
\n\n
This isn’t a behind-the-desk role. You’ll be present with patients, part of a team, and contributing to research that has real-world impact from day one.
\n\n
What You’ll Do
\n\n
Support the coordination of active clinical trials, including patient visits, scheduling, and study-related procedures
\nAssist with data collection and documentation, learning to apply the rigorous standards that clinical research demands
\nPerform and develop competency in clinical procedures including vital signs, EKGs, phlebotomy, and specimen processing
\nInteract directly with study participants – greeting them, explaining visit steps, and ensuring they feel supported throughout the process
\nWork closely with Clinical Research Coordinators and site leadership, asking questions, seeking feedback, and building your clinical knowledge base
\nContribute to a compliant, audit-ready site by following established protocols, SOPs, and Good Documentation Practices
\n\n
What We’re Looking For
\nYou don’t need to have done this exact job before. You need to be the kind of person who takes ownership of their work, communicates clearly, pays close attention to detail, and genuinely cares about the patient experience. The rest we’ll help you build.
\n\n
High school diploma or technical degree with 3+ years of relevant experience in life sciences, OR Associate’s degree with 1+ year of relevant experience, OR Bachelor’s degree with relevant coursework or experience in a clinical or life sciences setting
\nFamiliarity with medical terminology and basic clinical procedures is a plus
\nComfortable working in a fast-paced, team-based environment
\nProficient with standard computer tools; able to learn new systems quickly
\nICH-GCP and IATA certification required within a defined timeframe upon hire (we’ll support you through it)
\nPhysical Requirements & Work Environment
\nThis role is performed on-site at a clinical or office facility and requires prolonged periods of sitting, standing, or walking throughout the work environment
\nRequires the ability to communicate clearly in verbal and written forms and to read and interpret detailed materials
\nMust be able to navigate a clinical facility, including areas with limited space, and transport supplies or work materials as needed
\nMay be required to wear personal protective equipment (PPE) in accordance with facility protocols
\nTravel between company sites, meetings, or partner locations may be required
\nReasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the role
\n\n
Why Join Profound Research?
\nMeaningful Impact: Every role at Profound contributes to advancing medical knowledge and expanding therapeutic options for patients – the work we do here matters
\nProfessional Growth: We invest in our people through comprehensive training, certification support, and ongoing education to help you grow in your role and your career
\nLeadership & Advancement: Profound is a place where initiative is recognized. We actively support internal growth and create pathways for people to take on greater responsibility over time
\nCollaborative Culture: You’ll work alongside a team of dedicated professionals who are passionate about clinical research and committed to doing it well
\nFull Benefits Package: Competitive compensation, health insurance, PTO, retirement plan, and professional development support
\nDiverse Clinical Exposure: Work across multiple therapeutic areas and study phases, building a breadth of experience that’s rare in a single organization (for Clinical / Patient-Facing roles)
\nStart Your Career in Clinical Research
\nIf you’re curious about how new treatments reach patients, detail-oriented by nature, and energized by work that genuinely matters – this is where that career begins.
\n\n
As an Assistant Clinical Research Coordinator at Profound Research, you’ll work alongside experienced clinical research staff at one of our sites, supporting the day-to-day execution of clinical trials that give patients access to therapies they couldn’t otherwise reach. You’ll learn by doing – gaining hands-on experience in study coordination, patient interaction, data collection, and clinical procedures – with a clear path to grow into greater ownership and responsibility over time.
\n\n
This isn’t a behind-the-desk role. You’ll be present with patients, part of a team, and contributing to research that has real-world impact from day one.
\n\n
What You’ll Do
\n\n
Support the coordination of active clinical trials, including patient visits, scheduling, and study-related procedures
\nAssist with data collection and documentation, learning to apply the rigorous standards that clinical research demands
\nPerform and develop competency in clinical procedures including vital signs, EKGs, phlebotomy, and specimen processing
\nInteract directly with study participants – greeting them, explaining visit steps, and ensuring they feel supported throughout the process
\nWork closely with Clinical Research Coordinators and site leadership, asking questions, seeking feedback, and building your clinical knowledge base
\nContribute to a compliant, audit-ready site by following established protocols, SOPs, and Good Documentation Practices
\n\n
What We’re Looking For
\nYou don’t need to have done this exact job before. You need to be the kind of person who takes ownership of their work, communicates clearly, pays close attention to detail, and genuinely cares about the patient experience. The rest we’ll help you build.
\n\n
High school diploma or technical degree with 3+ years of relevant experience in life sciences, OR Associate’s degree with 1+ year of relevant experience, OR Bachelor’s degree with relevant coursework or experience in a clinical or life sciences setting
\nFamiliarity with medical terminology and basic clinical procedures is a plus
\nComfortable working in a fast-paced, team-based environment
\nProficient with standard computer tools; able to learn new systems quickly
\nICH-GCP and IATA certification required within a defined timeframe upon hire (we’ll support you through it)
\nStart Your Career in Clinical Research
\nIf you’re curious about how new treatments reach patients, detail-oriented by nature, and energized by work that genuinely matters – this is where that career begins.
\n\n
As an Assistant Clinical Research Coordinator at Profound Research, you’ll work alongside experienced clinical research staff at one of our sites, supporting the day-to-day execution of clinical trials that give patients access to therapies they couldn’t otherwise reach. You’ll learn by doing – gaining hands-on experience in study coordination, patient interaction, data collection, and clinical procedures – with a clear path to grow into greater ownership and responsibility over time.
\n\n
This isn’t a behind-the-desk role. You’ll be present with patients, part of a team, and contributing to research that has real-world impact from day one.
\n\n
What You’ll Do
\n\n
Support the coordination of active clinical trials, including patient visits, scheduling, and study-related procedures
\nAssist with data collection and documentation, learning to apply the rigorous standards that clinical research demands
\nPerform and develop competency in clinical procedures including vital signs, EKGs, phlebotomy, and specimen processing
\nInteract directly with study participants – greeting them, explaining visit steps, and ensuring they feel supported throughout the process
\nWork closely with Clinical Research Coordinators and site leadership, asking questions, seeking feedback, and building your clinical knowledge base
\nContribute to a compliant, audit-ready site by following established protocols, SOPs, and Good Documentation Practices
\n\n
What We’re Looking For
\nYou don’t need to have done this exact job before. You need to be the kind of person who takes ownership of their work, communicates clearly, pays close attention to detail, and genuinely cares about the patient experience. The rest we’ll help you build.
\n\n
High school diploma or technical degree with 3+ years of relevant experience in life sciences, OR Associate’s degree with 1+ year of relevant experience, OR Bachelor’s degree with relevant coursework or experience in a clinical or life sciences setting
\nFamiliarity with medical terminology and basic clinical procedures is a plus
\nComfortable working in a fast-paced, team-based environment
\nProficient with standard computer tools; able to learn new systems quickly
\nICH-GCP and IATA certification required within a defined timeframe upon hire (we’ll support you through it)
\nPhysical Requirements & Work Environment
\nThis role is performed on-site at a clinical or office facility and requires prolonged periods of sitting, standing, or walking throughout the work environment
\nRequires the ability to communicate clearly in verbal and written forms and to read and interpret detailed materials
\nMust be able to navigate a clinical facility, including areas with limited space, and transport supplies or work materials as needed
\nMay be required to wear personal protective equipment (PPE) in accordance with facility protocols
\nTravel between company sites, meetings, or partner locations may be required
\nReasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the role
\n\n
Why Join Profound Research?
\nMeaningful Impact: Every role at Profound contributes to advancing medical knowledge and expanding therapeutic options for patients – the work we do here matters
\nProfessional Growth: We invest in our people through comprehensive training, certification support, and ongoing education to help you grow in your role and your career
\nLeadership & Advancement: Profound is a place where initiative is recognized. We actively support internal growth and create pathways for people to take on greater responsibility over time
\nCollaborative Culture: You’ll work alongside a team of dedicated professionals who are passionate about clinical research and committed to doing it well
\nFull Benefits Package: Competitive compensation, health insurance, PTO, retirement plan, and professional development support
\nDiverse Clinical Exposure: Work across multiple therapeutic areas and study phases, building a breadth of experience that’s rare in a single organization (for Clinical / Patient-Facing roles)
\nStart Your Career in Clinical Research
\nIf you’re curious about how new treatments reach patients, detail-oriented by nature, and energized by work that genuinely matters – this is where that career begins.
\n\n
As an Assistant Clinical Research Coordinator at Profound Research, you’ll work alongside experienced clinical research staff at one of our sites, supporting the day-to-day execution of clinical trials that give patients access to therapies they couldn’t otherwise reach. You’ll learn by doing – gaining hands-on experience in study coordination, patient interaction, data collection, and clinical procedures – with a clear path to grow into greater ownership and responsibility over time.
\n\n
This isn’t a behind-the-desk role. You’ll be present with patients, part of a team, and contributing to research that has real-world impact from day one.
\n\n
What You’ll Do
\n\n
Support the coordination of active clinical trials, including patient visits, scheduling, and study-related procedures
\nAssist with data collection and documentation, learning to apply the rigorous standards that clinical research demands
\nPerform and develop competency in clinical procedures including vital signs, EKGs, phlebotomy, and specimen processing
\nInteract directly with study participants – greeting them, explaining visit steps, and ensuring they feel supported throughout the process
\nWork closely with Clinical Research Coordinators and site leadership, asking questions, seeking feedback, and building your clinical knowledge base
\nContribute to a compliant, audit-ready site by following established protocols, SOPs, and Good Documentation Practices
\n\n
What We’re Looking For
\nYou don’t need to have done this exact job before. You need to be the kind of person who takes ownership of their work, communicates clearly, pays close attention to detail, and genuinely cares about the patient experience. The rest we’ll help you build.
\n\n
High school diploma or technical degree with 3+ years of relevant experience in life sciences, OR Associate’s degree with 1+ year of relevant experience, OR Bachelor’s degree with relevant coursework or experience in a clinical or life sciences setting
\nFamiliarity with medical terminology and basic clinical procedures is a plus
\nComfortable working in a fast-paced, team-based environment
\nProficient with standard computer tools; able to learn new systems quickly
\nICH-GCP and IATA certification required within a defined timeframe upon hire (we’ll support you through it)
\nStart Your Career in Clinical Research
\nIf you’re curious about how new treatments reach patients, detail-oriented by nature, and energized by work that genuinely matters – this is where that career begins.
\n\n
As an Assistant Clinical Research Coordinator at Profound Research, you’ll work alongside experienced clinical research staff at one of our sites, supporting the day-to-day execution of clinical trials that give patients access to therapies they couldn’t otherwise reach. You’ll learn by doing – gaining hands-on experience in study coordination, patient interaction, data collection, and clinical procedures – with a clear path to grow into greater ownership and responsibility over time.
\n\n
This isn’t a behind-the-desk role. You’ll be present with patients, part of a team, and contributing to research that has real-world impact from day one.
\n\n
What You’ll Do
\n\n
Support the coordination of active clinical trials, including patient visits, scheduling, and study-related procedures
\nAssist with data collection and documentation, learning to apply the rigorous standards that clinical research demands
\nPerform and develop competency in clinical procedures including vital signs, EKGs, phlebotomy, and specimen processing
\nInteract directly with study participants – greeting them, explaining visit steps, and ensuring they feel supported throughout the process
\nWork closely with Clinical Research Coordinators and site leadership, asking questions, seeking feedback, and building your clinical knowledge base
\nContribute to a compliant, audit-ready site by following established protocols, SOPs, and Good Documentation Practices
\n\n
What We’re Looking For
\nYou don’t need to have done this exact job before. You need to be the kind of person who takes ownership of their work, communicates clearly, pays close attention to detail, and genuinely cares about the patient experience. The rest we’ll help you build.
\n\n
High school diploma or technical degree with 3+ years of relevant experience in life sciences, OR Associate’s degree with 1+ year of relevant experience, OR Bachelor’s degree with relevant coursework or experience in a clinical or life sciences setting
\nFamiliarity with medical terminology and basic clinical procedures is a plus
\nComfortable working in a fast-paced, team-based environment
\nProficient with standard computer tools; able to learn new systems quickly
\nICH-GCP and IATA certification required within a defined timeframe upon hire (we’ll support you through it)
\nPhysical Requirements & Work Environment
\nThis role is performed on-site at a clinical or office facility and requires prolonged periods of sitting, standing, or walking throughout the work environment
\nRequires the ability to communicate clearly in verbal and written forms and to read and interpret detailed materials
\nMust be able to navigate a clinical facility, including areas with limited space, and transport supplies or work materials as needed
\nMay be required to wear personal protective equipment (PPE) in accordance with facility protocols
\nTravel between company sites, meetings, or partner locations may be required
\nReasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the role
\n\n
Why Join Profound Research?
\nMeaningful Impact: Every role at Profound contributes to advancing medical knowledge and expanding therapeutic options for patients – the work we do here matters
\nProfessional Growth: We invest in our people through comprehensive training, certification support, and ongoing education to help you grow in your role and your career
\nLeadership & Advancement: Profound is a place where initiative is recognized. We actively support internal growth and create pathways for people to take on greater responsibility over time
\nCollaborative Culture: You’ll work alongside a team of dedicated professionals who are passionate about clinical research and committed to doing it well
\nFull Benefits Package: Competitive compensation, health insurance, PTO, retirement plan, and professional development support
\nDiverse Clinical Exposure: Work across multiple therapeutic areas and study phases, building a breadth of experience that’s rare in a single organization (for Clinical / Patient-Facing roles)
\nPhysical Requirements & Work Environment
\nThis role is performed on-site at a clinical or office facility and requires prolonged periods of sitting, standing, or walking throughout the work environment
\nRequires the ability to communicate clearly in verbal and written forms and to read and interpret detailed materials
\nMust be able to navigate a clinical facility, including areas with limited space, and transport supplies or work materials as needed
\nMay be required to wear personal protective equipment (PPE) in accordance with facility protocols
\nTravel between company sites, meetings, or partner locations may be required
\nReasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the role
\n\n
Why Join Profound Research?
\nMeaningful Impact: Every role at Profound contributes to advancing medical knowledge and expanding therapeutic options for patients – the work we do here matters
\nProfessional Growth: We invest in our people through comprehensive training, certification support, and ongoing education to help you grow in your role and your career
\nLeadership & Advancement: Profound is a place where initiative is recognized. We actively support internal growth and create pathways for people to take on greater responsibility over time
\nCollaborative Culture: You’ll work alongside a team of dedicated professionals who are passionate about clinical research and committed to doing it well
\nFull Benefits Package: Competitive compensation, health insurance, PTO, retirement plan, and professional development support
\nDiverse Clinical Exposure: Work across multiple therapeutic areas and study phases, building a breadth of experience that’s rare in a single organization (for Clinical / Patient-Facing roles)
\n