• Research Compliance Monitor

    Wayne State University (Detroit, MI)
    Research Compliance Monitor , IRB Wayne...For-Cause Audits as requested by the Institutional Review Board Committee or Human Research ... compliance . Submit monitoring reports to the Human Research Protection Program Administration and to the Institutional...and protocol violations and direct to committee Chair, individual Institutional Review Board , institutional more
    Wayne State University (11/08/25)
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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 ... responsibilities as assigned CRC-A + Prepare and process all Institutional Review Board ( IRB...institutional or study related committees and personnel (eg, IRB , DSMC, DSMB/Medical Monitor ) according to applicable… more
    University of Pennsylvania (10/03/25)
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  • Clinical Research Coordinator 3 (A)

    University of Miami (Miami, FL)
    …a proven experience in managing regulatory documentation and submissions to entities such as the Institutional Review Board ( IRB ) and the Food and Drug ... compliance and supporting the integrity of our clinical research efforts. + Assist PIs and study team with...initial study requests, annual reviews and modifications to the Institutional Review Board ( IRB more
    University of Miami (11/21/25)
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  • Clinical Research Coordinator 2

    Stanford University (Stanford, CA)
    …applicable regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions, ... and FDA regulations, Institutional Review Board requirements, and Good Clinical Practices. IRB submissions. + 2-4 years clinical research coordinator… more
    Stanford University (10/25/25)
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  • Research Director (GME) - Director…

    Henry Ford Health System (Southfield, MI)
    …informed consent processes, and human subjects protection principles. + Coordinate with the Institutional Review Board ( IRB ) to facilitate efficient ... role serves as the central point of coordination for research education, IRB and IACUC compliance..., Reporting, and Continuous Improvement + Monitor compliance with institutional research policies… more
    Henry Ford Health System (10/13/25)
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  • Regulatory Affairs Professional (Open Rank:…

    University of Colorado (Aurora, CO)
    …Experience with University of Colorado/UCHealth systems (Colorado Multiple Institutional Review Board , UCHealth Research Administration, Oncore, InfoED, ... Professional. The position will independently maintain and manage all IRB and regulatory processes for multi-site sponsored research...include, but not be limited to: submissions to the Institutional Review Board ( IRB more
    University of Colorado (11/09/25)
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  • Clinical Research Specialist - The Angeles…

    Cedars-Sinai (Los Angeles, CA)
    …federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board ( IRB ). **Primary Duties and ... aspects of research infrastructure development and/or maintenance. + Coordinates research projects at an institutional or departmental level. Serves as… more
    Cedars-Sinai (09/20/25)
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  • Clinical Research Coordinator A

    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 ... submissions and renewals in accordance with FDA and IRB guidelines + Assure compliance with the...of a team, as well as independently; knowledge of IRB and human research protection regulations; prior… more
    University of Pennsylvania (11/20/25)
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  • Clinical Research Coordinator 2 - Surgical…

    Stanford University (Stanford, CA)
    …applicable regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions, ... Human Subjects Panel. + Coordinate new protocol submissions, renewals, and revisions to Institutional Review Board for multiple studies. Complete annual… more
    Stanford University (10/07/25)
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  • Research Nurse (RN) - NIH

    Kelly Services (Bethesda, MD)
    …clinical and research information gained for purposes of communication with the Institutional Review Board and publication. * Assist in communication ... submitting and maintaining IRB , FDA, and/or other regulatory documents and research correspondence. * Monitor study enrollment goals and initiate strategies… more
    Kelly Services (11/22/25)
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