• Institutional Review Board

    Sanford Health (Sioux Falls, SD)
    IRB is never boring but always rewarding. **Job Summary** The Institutional Review Board ( IRB ) Specialist ensures submitted research is reviewed ... detailed in Sanford Institutional Review Board Policy. Serves in role of IRB ...of the IRB : to approve research, conduct protocol pre- review , require changes for IRB more
    Sanford Health (05/30/25)
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  • Research Nurse Specialist - Ambulatory

    Northwell Health (New York, NY)
    …adherence to established protocols to ensure projects are carried out as directed by the Institutional Review Board ( IRB ). Works within scope of practice ... Drug Administration (FDA), Good Clinical Practice, institutional policies, sponsor requirements, Institutional Review Board ( IRB ) and related… more
    Northwell Health (06/26/25)
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  • Regulatory Compliance Specialist - Medicine…

    Houston Methodist (Houston, TX)
    …laws, regulations, guidance, policy and procedure developed by Houston Methodist Research Institute Institutional Review Board ( IRB ), Food and Drug ... relationships with key study personnel. + Acts as a liaison between the institutional review committees, regulatory agencies, and the investigators to ensure… more
    Houston Methodist (04/06/25)
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  • Clinical Research Specialist - Albany, NY…

    Trinity Health (Albany, NY)
    …design and statistical analysis + Determines study-specific documentation requirements and prepares Institutional Review Board ( IRB ) submissions, ... and figures for anticipated publication/presentation Documentation Management: + Maintains protocol regulatory documents for compliance with IRB , including… more
    Trinity Health (06/24/25)
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  • Investigator Initiated Trial Specialist

    Stony Brook University (Stony Brook, NY)
    …Investigational New Drug (IND) and Investigational Device Exemption (IDE) applications. + Creating Institutional Review Board ( IRB ) submissions and ... Investigator Initiated Trial Specialist - Clinical Trials **Position Summary** The Cancer...managing correspondence across research sites, particularly in single- IRB /multi-site studies. + Planning and implementing changes to the… more
    Stony Brook University (05/31/25)
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  • Research Nurse Specialist II - Weekend…

    Vanderbilt University Medical Center (Nashville, TN)
    …Research Staff Council monthly meetings. + Attends in-services advertised by the Institutional Review Board , Research Support Services, professional ... prepares and processes new IRB research proposals, amendments, continuing review applications and adverse events according to institutional and departmental… more
    Vanderbilt University Medical Center (04/26/25)
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  • Clinical Research Specialist II - Clinical…

    Cedars-Sinai (Los Angeles, CA)
    …federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board ( IRB ). **Primary Duties and ... and collaborative, multi-site clinical research. The CCC Clinical Research Specialist II will serve in a cross-functional role and...including the Food and Drug Administration (FDA) and local Institutional Review Board . + Maintains… more
    Cedars-Sinai (06/25/25)
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  • Clinical Research Coordinator - A/B (Department…

    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 , ... Williams Syndrome. Clinical Research Coordinator work includes study design, protocol development, submission to review boards, subject...specialist in preparing for all local and Central Institutional Review Board ( IRB more
    University of Pennsylvania (05/04/25)
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  • Registered Nurse RN Clinical Research…

    Banner Health (Mesa, AZ)
    …through interactions with research staff, internal and external investigators, study sponsors and Institutional Review Board ( IRB ). 8. Participates in ... last for many years. As a **RN Clinical Research Specialist ** you play a crucial role in clinical trials,...of research, including patient care, data collection, and study protocol adherence. **Schedule:** Full-time, exempt, 40hrs week. Monday -… more
    Banner Health (04/16/25)
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  • Clinical Research Specialist

    Dignity Health (Phoenix, AZ)
    …Administration (FDA), Office for Human Research Protections (OHRP), Good Clinical Practices (GCP), Institutional Review Board ( IRB ), HIPAA regulations ... following duties: o Knowledge of all regulatory requirements and institutional requirements when conducting the study protocol (s)....to the Investigator as well as the sponsor and IRB in accordance to their requirements. o Coordinates research… more
    Dignity Health (06/07/25)
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