• CHET Outcomes Research Coordinator

    University of Rochester (Saunders County, NE)
    …and internal equity considerations._ **Responsibilities:** Coordinates the activities associated with human subject research . **SCHEDULE:** + 8 AM-5 PM; OCC ... more
    University of Rochester (03/13/25)
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  • Clinical Research Coordinator

    Mount Sinai Health System (New York, NY)
    …in the preparation and submission of grant applications and documents (eg, Institutional Review Board , Grants and Contracts Office). **Qualifications** ... more
    Mount Sinai Health System (03/28/25)
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  • Regulatory Coordinator - Surgery

    UCLA Health (Los Angeles, CA)
    …documents, and all required applications and forms + submissions to the applicable Institutional Review Board ( IRB ), informed consent form ... more
    UCLA Health (03/06/25)
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  • Human Subject Research

    University of Rochester (Rochester, NY)
    …interventional activities, to document adverse events and report to senior study staff, PI, Institutional Review Board ( IRB ), Sponsor, and/or any other ... more
    University of Rochester (03/17/25)
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  • Human Subject Research

    University of Rochester (Rochester, NY)
    …and internal equity considerations._ **Responsibilities:** Coordinates all aspects of assigned research studies associated with human subject research . ... more
    University of Rochester (03/17/25)
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  • Clinical Research Coordinator

    General Dynamics Information Technology (Portsmouth, VA)
    …Portsmouth (NMCP). The CRC is responsible for providing research coordination support for IRB - and IACUC -approved human and animal research protocols in ... more
    General Dynamics Information Technology (03/29/25)
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  • Human Subject Res Coordinator II,…

    University of Rochester (Rochester, NY)
    …or an equivalent combination of education and relevant experience required. - Experience as Human Subject Research Coordinator I preferred - Knowledge of ... more
    University of Rochester (03/17/25)
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  • Clinical Research Coordinator

    University of Colorado (Colorado Springs, CO)
    …are conducted in compliance with various regulations, including but not limited to Institutional Review Board ( IRB ), ClinicalTrials.gov, federal ... more
    University of Colorado (01/03/25)
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  • Human Subject Research Spec I

    University of Rochester (Rochester, NY)
    …with protocol requirements to document adverse events and report to senior study staff, PI, Institutional Review Board ( IRB ), Sponsor, and/or any other ... more
    University of Rochester (03/17/25)
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  • Human Subject Research Specialist II

    University of Rochester (Strong, AR)
    …works as an integral part of the research team. This role mentors Human Subject Research Coordinator I(s) and supervises students as assigned. ... more
    University of Rochester (03/19/25)
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  • Human Subject Research Specialist II

    University of Rochester (Rochester, NY)
    …works as an integral part of the research team. This role mentors Human Subject Research Coordinator I(s) and supervises students as assigned. TYPICAL ... more
    University of Rochester (03/17/25)
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  • Human Sub Research Spec II

    University of Rochester (Rochester, NY)
    …and consent form development, budget development, negotiation and implementation, discussions with the human subjects review board and the University's legal ... more
    University of Rochester (03/17/25)
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  • Human Subject Research Specialist I

    University of Rochester (Strong, AR)
    …degree, or required. + Associate's degree and completion of 6 months in the Human Subject Research Coordinator Trainee program, + Equivalent combination of ... more
    University of Rochester (02/13/25)
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  • Clinical Research Coordinator - A/B…

    University of Pennsylvania (Philadelphia, PA)
    … B will assist the regulatory specialist in preparing for all local and Central Institutional Review Board ( IRB ) documentation through the IRB ... more
    University of Pennsylvania (03/09/25)
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  • Clinical Research Coordinator A/B…

    University of Pennsylvania (Philadelphia, PA)
    …in the field of lipoprotein metabolism, atherosclerosis, and cardiovascular disease. Assist with Institutional Review Board ( IRB ) filings and inquiries, ... more
    University of Pennsylvania (02/14/25)
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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 ... more
    University of Pennsylvania (03/09/25)
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  • Clinical Research Coordinator I…

    Cedars-Sinai (Los Angeles, CA)
    …Administration (FDA) and local Institutional Review Board ( IRB ). **Primary Duties and Responsibilities:** + Schedules research visits and procedures ... more
    Cedars-Sinai (03/10/25)
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  • Clinical Research Coordinator

    Nuvance Health (Danbury, CT)
    … patient, protocol implementation, data collection and query resolution, and submission to the Institutional Review Board ( IRB ). Coordinates studies in ... more
    Nuvance Health (03/12/25)
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  • Research Program Coordinator

    Johns Hopkins University (Baltimore, MD)
    IRB requirements, and facilitates IRB audits. + Interacts with Johns Hopkins Institutional Review Board and staff. + Enters e- irb protocols and ... more
    Johns Hopkins University (02/20/25)
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  • Clinical Research Coordinator

    Nuvance Health (Poughkeepsie, NY)
    … patient, protocol implementation, data collection and query resolution, and submission to the Institutional Review Board ( IRB ). Coordinates studies in ... more
    Nuvance Health (03/22/25)
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