• Institutional Review Board

    University of Texas Rio Grande Valley (Mcallen, TX)
    …to protect their safety, rights, and welfare in compliance with Institutional Review Board ( IRB ) regulations for the Human Subjects Protections ... university's Human Subjects Protections Program and communicates with the Institutional Review Board regarding the...research and other aspects of research compliance . Ability to apply regulatory review criteria… more
    University of Texas Rio Grande Valley (08/08/25)
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  • Administrator - Institutional Review

    HonorHealth (AZ)
    …Job Summary Coordinates all activities related to the Institutional Review Board and assures compliance with IRB guidelines and FDA regulations. In ... the IRB Coordinator facilitates initial and continuing review of research protocols in compliance...This includes initial determinations regarding expedited, exempt, or full board review , as well as human subject… more
    HonorHealth (07/30/25)
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  • Program Specialist - Institutional

    University of Texas Rio Grande Valley (Mcallen, TX)
    …activities and resolutions of human subjects' research applications in coordination with the Institutional Review Board ( IRB ) Coordinators. + ... Position Information Posting NumberSRGV8449 Working TitlePROGRAM SPECIALIST - INSTITUTIONAL REVIEW BOARD COORDINATOR...subjects' research administration within the Office of Research Compliance . Description of Duties + Coordinates… more
    University of Texas Rio Grande Valley (08/08/25)
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  • Human Research Protection Program (HRPP)…

    Brown University (Providence, RI)
    …administration and implementation of the Human Research Protection Program (HRPP) and Institutional Review Board ( IRB ) policies and procedures ... the Human Research Protection Program (HRPP) and Institutional Review Board ( IRB...least 3 years of related experience working in a research compliance setting, either in administration or… more
    Brown University (07/27/25)
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  • Clinical Research Regulatory Specialist

    University of Southern California (Los Angeles, CA)
    …Submits protocols and supporting documents to internal and external regulatory bodies (ie Institutional Review Board ), ensuring trials are consistent with ... Supervises:No Preferred Field of Expertise:Three years' experience in clinical research compliance , regulatory research and/or...academic or private sector. Experience with submissions to the Institutional Review Board and/or the… more
    University of Southern California (07/11/25)
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  • Associate Human Research Protection Program…

    Brown University (Providence, RI)
    …administration and implementation of the Human Research Protection Program (HRPP) and Institutional Review Board ( IRB ) policies and procedures ... , Brown will soon be the main HRPP and Institutional Review Board ( IRB...least 1 year of related experience working in a research compliance setting, either in administration or… more
    Brown University (05/12/25)
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  • Institutional Review Board

    Geisinger (Danville, PA)
    …procedural guidance for regulatory and compliance issues. Provides technical support for Institutional Review Board system users and serve as a liaison ... compliance with regulatory requirements, institutional and Institutional Review Board policies and...research . + Administers educational programs pertaining to human research protections and IRB review more
    Geisinger (06/25/25)
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  • Manager, Research Operations

    Community Health Systems (Franklin, TN)
    …limited to NIH, JCAHO, OSHA, FDA, HIPAA, OIG, IRB . Collaborates with institutional compliance efforts related to research matters to ensure completion ... build in the Clinical Trial Management System, agreements, and Institutional Review Board submission) and...**Licenses and Certifications** + CHRC - Certified in Healthcare Research Compliance preferred or + CCRP -… more
    Community Health Systems (07/11/25)
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  • Sr. Director Research - Administration…

    Guthrie (Sayre, PA)
    …high-performing teams. Operations & Compliance + Deep understanding of human-subjects research compliance (AAHRPP, FDA, IRB , GCP, ICH). + Experience ... has broad oversight responsibilities across core domains: + Clinical Research Operations in compliance and in regulatory...operations align with federal (OHRP, FDA), state laws and institutional policies. Provides guidance to the IRB more
    Guthrie (05/14/25)
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  • PS Clinical Research Coord

    University of Utah (Salt Lake City, UT)
    …to have two years related experience and possess a nationally recognized research compliance certification. This position is patient-sensitive and must fulfill ... enrollment goals and initiates strategies to promote enrollment and participant compliance . Coordinates and performs responsibilities related to research more
    University of Utah (08/07/25)
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