• 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 ... assigned. **Education** + Bachelor's Degree **Experience** Approximately 3 years of IRB regulatory experience or research management experience. Working… more
    Weill Cornell Medical College (07/10/25)
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  • Clinical Research Associate I

    Stony Brook University (Stony Brook, NY)
    …various internal and external constituents including sponsors, cooperative groups, Institutional Review Board and regulatory agencies. + May assist the ... review (ie Cerner Powerchart). Experience working with an IRB (Investigational Review Board ) for...conferences and research meetings. + Assure timely communication of regulatory documents to the IRB . Report Serious… more
    Stony Brook University (08/02/25)
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  • Investigator Initiated Trial Specialist - Clinical…

    Stony Brook University (Stony Brook, NY)
    …Investigational New Drug (IND) and Investigational Device Exemption (IDE) applications. + Creating Institutional Review Board ( IRB ) submissions and ... The Investigator Initiated Trial Specialist provides operational support and regulatory management for investigator-initiated clinical research at Stony Brook Cancer… more
    Stony Brook University (05/31/25)
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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 ... and/or brain stimulation as a research tool. Experience with preparation of regulatory materials (eg, IRB , grant progress reports). Experience with purchasing,… 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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  • Research Program Coordinator II-Radiology

    Mount Sinai Health System (New York, NY)
    …operational and statistical reports for the PI and/or regulatory agencies. 10. Completes all Institutional Review Board ( IRB ) or IACUC and other ... and records observations on progress of research, investigations and data per regulatory requirements and MSMC protocols. 5. Establishes goals and objectives for… more
    Mount Sinai Health System (07/27/25)
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  • Human Subject Research Specialist II

    University of Rochester (Rochester, NY)
    …managing and supervising staff, working with familycaregiversand/orproviders, preparing and managing Institutional Review Board documentation preferred. + ... in research policies and practices, professional development, and performance. Manages regulatory paperwork in accordance with human subject IRB , continuing… more
    University of Rochester (08/07/25)
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  • Clinical Research Coordinator I- Pulmonary

    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). ... Under Supervision of the Principal Investigator(s). + Ensure Proper Compliance with Institutional and Regulatory Requirements. + Attends weekly ILD meeting. +… more
    Mount Sinai Health System (07/25/25)
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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** ... REDCap database. + May assist in the preparation for regulatory agency site visits. + Assists with IRB... regulatory agency site visits. + Assists with IRB submissions. + Other duties as assigned. **About Us**… 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 ... to immediate team members and relevant others. + Tracks regulatory and other documents, such as consent forms and...and ensures these are complete, accurate and available for review . + Learns and applies the details of the… more
    University of Rochester (08/07/25)
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