• IRB Coordinator (Office of Human Subjects…

    Johns Hopkins University (Baltimore, MD)
    …who will be part of a team that processes human subjects research protocols overseen by the Institutional Review Board ( IRB ). The IRB Coordinator is ... 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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  • Senior Director IRB

    Cleveland Clinic (Cleveland, OH)
    …you will lead the Cleveland Clinic Human Subjects Protection Program and oversee all Institutional Review Board ( IRB ) operations, including policies, ... the enterprise. This role is responsible for the development, review and approval of IRB policies and...overseeing staff and ensuring adherence to federal, state and institutional policies + Collaborative mindset to work with researchers… more
    Cleveland Clinic (12/19/25)
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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 ... human subjects research. This role supports investigators, staff, and IRB members in the preparation, review , and...members. + Maintain compliance with OHRP, FDA, ICH/GCP, and institutional regulations. + Manage IRB databases, tracking… 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 ... of IRB applications, maintenance of IRB files, preparation of IRB approval letters, initial application support, and pre- review activities. + Perform… more
    BayCare Health System (11/18/25)
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  • Hrpp/ IRB Office (Research, Regulatory,…

    UTMB Health (Galveston, TX)
    …Coordinates regulatory committee reviews of human subjects/animal protocols, including management of Institutional Review Board ( IRB ) committee/ ... HRPP/ IRB Office (Research, Regulatory, & Compliance - Galveston)...of protocol review management to assist the Institutional Review Board / Institutional more
    UTMB Health (11/26/25)
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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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  • IRB Compliance Monitoring Specialist…

    Johns Hopkins University (Baltimore, MD)
    …written reports of monitoring findings and recommendations for review by the Institutional Review Board . + Participate in Compliance Monitoring Program ... We are seeking an ** IRB Compliance Monitoring Specialist** who will be part...be part of a team that supports the JHM Institutional Review Boards (IRBs). This role conducts… more
    Johns Hopkins University (12/24/25)
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  • IRB Administrator / TSRI- Human Research…

    Children's Hospital Los Angeles (Los Angeles, CA)
    …Subjects Protection Program in the areas of protocol reviews, liaison with the Institutional Review Board , and simple to moderately complex correspondence. ... **Minimum Qualifications/Work Experience:** 1+ years IRB experience. **Education/Licensure/Certification:** Bachelor's degree in a scientific or business discipline… more
    Children's Hospital Los Angeles (12/25/25)
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  • Human Research Protection Program (HRPP)…

    Brown University (Providence, RI)
    …of the BIRCH initiative (http://birch.brown.edu/) , Brown will soon be the main HRPP and Institutional Review Board ( IRB ) of record for Brown, Lifespan ... administration and implementation of the Human Research Protection Program (HRPP) and Institutional Review Board ( IRB ) policies and procedures related to… more
    Brown University (10/26/25)
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  • Clinical Research Associate I (Hybrid, Per Diem)…

    Cedars-Sinai (Los Angeles, CA)
    …for long term follow-up patients only. + Assists with regulatory submissions to the Institutional Review Board ( IRB ) including submission of Adverse ... participants. **5%** - Assists supervising staff with regulatory submissions to the Institutional Review Board ( IRB ), including the submission of Adverse… more
    Cedars-Sinai (12/21/25)
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  • Clinical Research Associate I - Yang Lab - Karsh…

    Cedars-Sinai (Beverly Hills, CA)
    …report forms (CRFs), entering clinical research data, and assisting with regulatory submissions to the Institutional Review Board ( IRB ). The CRA I member ... long term follow-up patients only. + Assists with regulatory submissions to the Institutional Review Board ( IRB ) and works closely with supervising… more
    Cedars-Sinai (12/25/25)
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  • Clinical Research Coordinator II, Thoracic…

    Cedars-Sinai (Beverly Hills, CA)
    …federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board ( IRB ). Primary Duties and ... study conduct. Works closely with a regulatory coordinator or directly with the Institutional Review Board ( IRB ) to submit Adverse Events, Serious… more
    Cedars-Sinai (12/17/25)
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  • Clinical Research Coordinator II, Hybrid

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

    Cedars-Sinai (Los Angeles, CA)
    …federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board ( IRB ). **Primary Duties & ... conduct. + Works closely with a regulatory coordinator or directly with the Institutional Review Board ( IRB ) to submit Adverse Events, Serious Adverse… more
    Cedars-Sinai (11/21/25)
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  • Clinical Research Coordinator I - Guerin…

    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 ... conduct. + Works closely with a regulatory coordinator or directly with the Institutional Review Board ( IRB ) to submit Adverse Events, Serious Adverse… more
    Cedars-Sinai (11/08/25)
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  • Surgery Chair Clinical Research Coordinator II

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

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

    Brown University (Providence, RI)
    …of the BIRCH initiative (http://birch.brown.edu/) , Brown will soon be the main HRPP and Institutional Review Board ( IRB ) of record for Brown, Lifespan ... administration and implementation of the Human Research Protection Program (HRPP) and Institutional Review Board ( IRB ) policies and procedures related to… more
    Brown University (11/10/25)
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  • Heart Institute Clinical Research Associate I…

    Cedars-Sinai (Los Angeles, CA)
    …patient contact for long term follow-up patients only. Assists with regulatory submissions to the Institutional Review Board ( IRB ) and works closely with ... research data, and assist with regulatory submissions to the IRB . Provides limited patient contact as needed for study...supervising research staff or directly with the Institutional Review Board to submit… more
    Cedars-Sinai (11/28/25)
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