• Research Pharmacist - School of Medicine,…

    Emory Healthcare/Emory University (Atlanta, GA)
    …investigational or marketed drugs. + Serves as a representative of Emory University on the Institutional Review Board ( IRB ) to assist in protocol ... **Discover Your Career at Emory University** Emory University is a leading research university that fosters excellence and attracts world-class talent to innovate… more
    Emory Healthcare/Emory University (09/12/25)
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  • Supervisor- Research Compliance- Full time-…

    Henry Ford Health System (Detroit, MI)
    GENERAL SUMMARY: + Coordinates the administration of the Institutional Review Board ( IRB ), the Institutional Animal Care and Use Committee (IACUC), ... (IRDBC), and other regulatory activities and operational procedures involved with the review of research protocols. + The job responsibilities require an… more
    Henry Ford Health System (09/25/25)
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  • Clinical Research Data Specialist I…

    Cedars-Sinai (Los Angeles, CA)
    …agencies including the Food and Drug Administration (FDA) and local Institutional Review Board . Maintains research practices using Good Clinical Practice ... is home to some of the most advanced biomedical research and training programs in the world, which attracts...including the Food and Drug Administration (FDA) and local Institutional Review Board . **ESSENTIAL JOB… more
    Cedars-Sinai (10/12/25)
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  • Regulatory Compliance Specialist

    Houston Methodist (Houston, TX)
    …regulations, guidance, policy and procedure developed by Houston Methodist Research Institute Institutional Review Board ( IRB ), Food and Drug ... study personnel. + Acts as a liaison between the institutional review committees, regulatory agencies, and the...and applicable regulations. + Assists in the preparation of research protocols for IRB submission, submitting protocol… more
    Houston Methodist (07/29/25)
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  • Senior QA/RA Specialist

    Charles River Laboratories (Northridge, CA)
    …will also oversee the management of regulatory documentation related to the organization's Institutional Review Board ( IRB ) activities. Will assist ... quality cellular material and services to biotech and pharmaceutical companies and research organizations that are performing innovative research and developing… more
    Charles River Laboratories (09/24/25)
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  • Regulatory Specialist

    Weill Cornell Medical College (New York, NY)
    …and submits all necessary documents to the Clinical Science Evaluation Committee (CSEC), the Institutional Review Board ( IRB ) and ancillary committees. + ... IRB . + Performs central subject registration for specified research studies. + Reports all Serious Adverse Events (SAEs)...+ Reports all Serious Adverse Events (SAEs) to the Institutional Review Board and other… more
    Weill Cornell Medical College (10/21/25)
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  • Clinical Research Coordinator (CRC)

    General Dynamics Information Technology (Portsmouth, VA)
    …at the Naval Medical Center Portsmouth (NMCP). The CRC is responsible for providing research coordination support for IRB - and IACUC -approved human and animal ... by the government entity may be required for safety reasons. + Coordinate research activities of assigned IRB and IACUC-approved study protocols, such as… more
    General Dynamics Information Technology (09/23/25)
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  • Contractual -Registered Nurse-Part -Time

    University of Maryland, Baltimore (Baltimore, MD)
    …protocol worksheets, procedural manuals, adverse event reports, case report forms, and institutional review board documents. Conducts quality assurance ... research operations with protocols and all relevant local, federal , and state regulatory and institutional policies....Maryland license in good standing issued by the Maryland Board of Nursing to practice as a registered nurse… more
    University of Maryland, Baltimore (08/14/25)
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  • Sr. Clinical Research Coordinator-Emergency…

    Beth Israel Lahey Health (Boston, MA)
    …for participation in multiple clinical trials, ensuring compliance with federal , state and institutional guidelines. Financial responsibilities including ... submits protocols, amendments, notices, suspensions and terminations to the IRB for review and approval. (essential) +...with patients. Revises protocol consent form to comply with federal , state and IRB guidelines. (essential) +… more
    Beth Israel Lahey Health (08/09/25)
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  • Regulatory Coordinator - HM Pediatrics

    Dana-Farber Cancer Institute (Brookline, MA)
    …applications, amendments, continuing reviews, and informed consent documents for SRC and IRB review and approval + Prepares and submits regulatory documentation ... groups, clinical trials experts, representatives from the pharmaceutical industry, federal agencies, and other research organizations. Works interactively… more
    Dana-Farber Cancer Institute (09/13/25)
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