• Senior IRB Analyst

    Weill Cornell Medical College (New York, NY)
    …Has ability to independently assess submissions for category determination and each level of IRB review (pre- review , re- review , clarifying issues, post ... IRB meetings, including making assignments to staff and Board members, obtaining quorum for the meeting and providing...at the meeting and writing minutes. + Works with IRB leadership to review , develop and implement… more
    Weill Cornell Medical College (07/10/25)
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  • Clinical Research Associate I

    Stony Brook University (Stony Brook, NY)
    …correspond with various internal and external constituents including sponsors, cooperative groups, Institutional Review Board and regulatory agencies. + May ... review (ie Cerner Powerchart). Experience working with an IRB (Investigational Review Board ) for research protocol submissions, amendments and reviews.… more
    Stony Brook University (08/02/25)
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  • Research Support Specialist

    Stony Brook University (Stony Brook, NY)
    …protocol documents when required, manage medical charts, and ensure compliance with all Institutional Review Board policies. The successful incumbent must ... as a research tool. Experience with preparation of regulatory materials (eg, IRB , grant progress reports). Experience with purchasing, and/or budget management and… more
    Stony Brook University (08/08/25)
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  • Postdoctoral Associate

    Stony Brook University (Stony Brook, NY)
    …PET studies, available radiotracers for clinical/pre-clinical studies, setting up study protocols with Institutional Review Board ( IRB ), Radioactive Drug ... and synthesize/interpret results for internal and external presentation. * Correspond with the IRB and RDRC for existing and new PET studies. * Implement protocols… more
    Stony Brook University (08/02/25)
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  • Clinical Research Coordinator I-Addiction…

    Mount Sinai Health System (New York, NY)
    …study information. Assists in preparing grant applications and documents (for eg, Institutional Review Board , Grants and Contracts Office). ... agency, administering lifestyle questionnaires. + Assists in preparing grant applications, IRB /GCO for submission and filings. + Maintains source documents and… more
    Mount Sinai Health System (08/15/25)
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  • Research Program Coordinator I - Cardiology

    Mount Sinai Health System (New York, NY)
    …and proposals by developing pilot studies and generating pre-clinical data. + Completes all Institutional Review Board ( IRB ) or IACUC and other ... regulatory applications and renewals. + Develops consent forms, screens and enrolls patients, follows patients through course of study, collects and analyze data. (Clinical Research only) + Develops policies and procedures within area of responsibility. Writes… more
    Mount Sinai Health System (08/15/25)
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  • Research Assistant

    Weill Cornell Medical College (New York, NY)
    …of research data. + Assists in the preparation of materials, submissions and renewals to the Institutional Review Board ( IRB ) or IACUC. + Assists faculty ... in the preparation of grant submissions and associated documentation, which may include just-in-time documents, progress reports, routing forms, abstracts and manuscripts. + Performs other related duties as directed. **Education** + High School Diploma… more
    Weill Cornell Medical College (08/14/25)
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  • Associate Researcher I- Immunology…

    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** ... assist in the preparation for regulatory agency site visits. + Assists with IRB submissions. + Other duties as assigned. **About Us** **Strength through Unity and… more
    Mount Sinai Health System (08/08/25)
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  • Human Subj Res Coord Trainee

    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 ... consent forms and CRFs, and ensures these are complete, accurate and available for review . + Learns and applies the details of the protocol, including inclusion and… more
    University of Rochester (08/07/25)
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  • Human Subject Research Coordinator I

    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 ... such as consent forms and CRFs, are complete, accurate, and available for review . Communicates with Sponsor to clarify data queries to determine report format.… more
    University of Rochester (08/07/25)
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