• University Health (Seguin, TX)
    Senior Clinical Research Coordinator Please read the following job description thoroughly to ensure you are the right fit for this role before applying. Location: ... At University Health, we're seeking a Senior Clinical Research Coordinator to lead and support high-impact studies that shape...play a vital leadership role in the coordination and review of complex human subject research protocols. You will:… more
    JobLookup XML (12/15/25)
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  • University Health (Seguin, TX)
    …required for Research Proposals within University Health. Represents the department at multi- institutional committees and meetings, such as IRB and OHRP. ... you are a good match, make an application. The Senior Clinical Research Coordinator leads the evaluation of research protocols and provides clinical and risk… more
    JobLookup XML (12/15/25)
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  • University Health (San Antonio, TX)
    Senior Clinical Research Coordinator Location: University Health Full-Time - Day Shift Advance the Future of Clinical Research Are you passionate about clinical ... At University Health, we're seeking a Senior Clinical Research Coordinator to lead and support high-impact studies that shape...play a vital leadership role in the coordination and review of complex human subject research protocols. You will:… more
    job goal (12/22/25)
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  • IRB Coordinator (Office of Human…

    Johns Hopkins University (Baltimore, MD)
    …research protocols overseen by the Institutional Review Board ( IRB ). The IRB Coordinator is responsible for providing administrative support and ... Duties & Responsibilities** + Demonstrate knowledge-based understanding of the complete IRB review process. + Provide administrative support and advice… more
    Johns Hopkins University (12/24/25)
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  • IRB Coordinator Consultant

    Vitalief (Livingston, NJ)
    …will support a leading hospital research center in Livingston, NJ, administering and overseeing Institutional Review Board ( IRB ) activities to ensure ... grow sustainably. The Role We are seeking an experienced IRB Coordinator Consultant to join the Vitalief...human subjects research. This role supports investigators, staff, and IRB members in the preparation, review , and… more
    Vitalief (10/05/25)
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  • IRB Coordinator

    BayCare Health System (Clearwater, FL)
    …**Facility:** BayCare Systems Office (Hybrid) **Responsibilities:** + Provide functional support to the Institutional Review Board ( IRB ). + Responsible ... - 5:00PM **Weekend Work:** None **Equal Opportunity Employer Veterans/Disabled** **Position** IRB Coordinator **Location** Clearwater:BayCare Sys Office West |… more
    BayCare Health System (11/18/25)
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  • IRB Panel Coordinator

    University of Colorado (Aurora, CO)
    …** **Description** **University of Colorado Anschutz Medical Campus** **Department: Colorado Multiple Institutional Review Board - Office of Regulatory ... a year for year basis. **Preferred Qualifications:** + Experience working with Institutional Review Boards or OHRP/FDA regulations regarding human subject… more
    University of Colorado (11/21/25)
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  • Research Services Senior Clinical Science…

    University of Colorado (Aurora, CO)
    …employment in an academic medical research environment + Experience submitting protocols to an institutional review board ( IRB ) + REDCap development and ... and using structured process improvement methods; and experience developing and submitting institutional review board protocols for community-based studies.… more
    University of Colorado (12/25/25)
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  • Clinical Research Coordinator III…

    Cedars-Sinai (Los Angeles, CA)
    …study conduct. + Works closely with a regulatory coordinator or directly with the Institutional Review Board ( IRB ) to submit Adverse Events, Serious ... all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board ( IRB ). **Primary Job Duties and… more
    Cedars-Sinai (11/02/25)
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  • Clinical Research Coordinator II, Thoracic…

    Cedars-Sinai (Beverly Hills, CA)
    …study conduct. Works closely with a regulatory coordinator or directly with the Institutional Review Board ( IRB ) to submit Adverse Events, Serious ... must reside in the commutable area.** The Clinical Research Coordinator II works independently providing study coordination including screening...including the Food and Drug Administration (FDA) and local Institutional Review Board ( IRB more
    Cedars-Sinai (12/17/25)
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  • Clinical Research Coordinator II, Hybrid

    Cedars-Sinai (Beverly Hills, CA)
    …study conduct. + Works closely with a regulatory coordinator or directly with the Institutional Review Board ( IRB ) to submit Adverse Events, Serious ... **Job Description** The Clinical Research Coordinator II works independently providing study coordination including...including the Food and Drug Administration (FDA) and local Institutional Review Board ( IRB more
    Cedars-Sinai (12/13/25)
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  • Clinical Research Coordinator II - Guerin…

    Cedars-Sinai (Los Angeles, CA)
    …study conduct. + Works closely with a regulatory coordinator or directly with the Institutional Review Board ( IRB ) to submit Adverse Events, Serious ... you be doing in this role?** The Clinical Research Coordinator II works independently providing study coordination including screening...including the Food and Drug Administration (FDA) and local Institutional Review Board ( IRB more
    Cedars-Sinai (11/21/25)
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  • Clinical Research Coordinator I - Guerin…

    Cedars-Sinai (Los Angeles, CA)
    …study conduct. + Works closely with a regulatory coordinator or directly with the Institutional Review Board ( IRB ) to submit Adverse Events, Serious ... federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board ( IRB ). **Primary Duties and… more
    Cedars-Sinai (11/08/25)
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  • Surgery Chair Clinical Research Coordinator

    Cedars-Sinai (CA)
    …study conduct. + Works closely with a regulatory coordinator or directly with the Institutional Review Board ( IRB ) to submit Adverse Events, Serious ... federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board ( IRB ). **Primary Duties &… more
    Cedars-Sinai (11/05/25)
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  • Clinical Research Coordinator A/B

    University of Pennsylvania (Philadelphia, PA)
    …biological samples and related study documents, and collection of clinical data. Assist with Institutional Review Board ( IRB ) filings and inquiries, and ... resources, and much more. Posted Job Title Clinical Research Coordinator A/B Job Profile Title Clinical Research Coordinator...responsibilities as assigned CRC-A + Prepare and process all Institutional Review Board ( IRB more
    University of Pennsylvania (10/03/25)
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  • Research Coordinator II

    University of Southern California (Los Angeles, CA)
    …research is performed as described in protocol. Serves as contact for subjects, study personnel, Institutional Review Board ( IRB ) and study sponsor. + ... at Keck School of Medicine is seeking a Research Coordinator . Working directly under the supervision of Dr. Linda...study continuing review and study amendments to Institutional Review Board ( IRB more
    University of Southern California (11/19/25)
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  • Clinical Research Coordinator - Heart…

    WellSpan Health (York, PA)
    …care personnel and patients. Assists resident physicians with required scholarly activity ( Institutional Review Board ( IRB ) submission, presentations, ... protocols. Transmits and distributes protocol information, including protocol amendments, to the Institutional Review Board ( IRB ), physicians and… more
    WellSpan Health (12/24/25)
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  • Clinical Research Coordinator II - Research…

    Cedars-Sinai (Los Angeles, CA)
    …study conduct. + Works closely with a regulatory coordinator or directly with the Institutional Review Board ( IRB ) to submit Adverse Events, Serious ... the greatest needs in our region. The Clinical Research Coordinator II works independently providing study coordination including screening...including the Food and Drug Administration (FDA) and local Institutional Review Board ( IRB more
    Cedars-Sinai (12/05/25)
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  • Clinical Research Coordinator 2

    Stanford University (Stanford, CA)
    …bodies, which include HIPAA and FDA regulations, Institutional Review Board requirements, and Good Clinical Practices. IRB submissions. + 2-4 years ... Clinical Research Coordinator 2 **School of Medicine, Stanford, California, United...provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions, and… more
    Stanford University (10/25/25)
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  • Regulatory Coordinator - Georgetown…

    Georgetown Univerisity (Washington, DC)
    …frequent communication with the Institutional Review Board ( IRB ) and compliance offices. The Regulatory Coordinator often serves as the primary ... difference in the world. Requirements Job Overview The Regulatory Coordinator plays a critical role in ensuring regulatory compliance...trial sponsors, Office of Human Subjects Protection, Office of Institutional Review Board and Office… more
    Georgetown Univerisity (12/13/25)
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