• Clinical Research Regulatory Specialist

    University of Southern California (Los Angeles, CA)
    …Submits protocols and supporting documents to internal and external regulatory bodies (ie Institutional Review Board ), ensuring trials are consistent with ... and/or operations in the academic or private sector. Experience with submissions to the Institutional Review Board and/or the Federal Drug Administration for… more
    University of Southern California (07/11/25)
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  • Regulatory Compliance Specialist

    Houston Methodist (Houston, TX)
    …laws, regulations, guidance, policy and procedure developed by Houston Methodist Research Institute Institutional Review Board ( IRB ), Food and Drug ... At Houston Methodist, the Regulatory Compliance Specialist position is responsible for coordinating and performing...study personnel. + Acts as a liaison between the institutional review committees, regulatory agencies, and the… more
    Houston Methodist (07/29/25)
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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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  • Clinical Research Specialist

    University of Maryland, Baltimore (Baltimore, MD)
    …position significantly contributes to the conduct of research. * Coordinates the preparation of Institutional Review Board ( IRB ) and Health Insurance ... Center (UMGCCC) is currently recruiting for a full-time Bone Marrow Research Specialist (Clinical Research Specialist ).* Following an extensive training program,… more
    University of Maryland, Baltimore (07/22/25)
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  • Clinical Research Specialist

    University of Maryland, Baltimore (Baltimore, MD)
    …position significantly contributes to the conduct of research. * Coordinates the preparation of Institutional Review Board ( IRB ) and Health Insurance ... (UMGCCC) has an exciting opportunity for a full-time Clinical Research Specialist for the Hematologic Malignancies research program.*This position will be… more
    University of Maryland, Baltimore (07/22/25)
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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 Specialist

    University of Maryland, Baltimore (Baltimore, MD)
    …position significantly contributes to the conduct of research. * Coordinates the preparation of Institutional Review Board ( IRB ) and Health Insurance ... Maryland, Baltimore (UMB) is currently seeking a Clinical Research Specialist .* Accomplishes responsibilities by applying specialized and theoretical knowledge,… more
    University of Maryland, Baltimore (07/10/25)
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  • Pathology Specialist

    Veterans Affairs, Veterans Health Administration (White River Junction, VT)
    …harvest normal, pre-neoplastic, and abnormal (tumor) tissue from surgical specimens for all Institutional Review Board ( IRB )-approved research protocols ... Summary The position serves as a Pathology Specialist in Pathology and Laboratory Medicine Service within...Complies with regulations guiding tissue repositories, patient privacy, and institutional review boards. Performs additional duties as… more
    Veterans Affairs, Veterans Health Administration (07/31/25)
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  • Sr. Compliance Monitoring Specialist

    Johns Hopkins University (Fort Defiance, AZ)
    …and institutional policies that must be corrected prior to IRB review . + Determine that appropriate protocol and application-specific documentation ... a **_Sr. Compliance Monitoring Specialist_** . There are several Institutional Review Boards (IRBs) that we report...the FDA or commercial sponsors. + Assist in the review of IRB action outcomes, including the… more
    Johns Hopkins University (07/11/25)
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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 (07/26/25)
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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,...that includes the da Vinci Surgical System. Becker's Hospital Review named Banner Desert Medical Center as one of… more
    Banner Health (07/24/25)
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  • Clinical Study Documentation Specialist

    Caris Life Sciences (Phoenix, AZ)
    …and industry best practices. Responsibilities include maintaining study documentation, coordinating Institutional Review Board ( IRB ) submissions, ... Associates degree + 2 years experience with preparing and submitting documents to Institutional Review Boards (IRBs). + Strong understanding of clinical research… more
    Caris Life Sciences (06/25/25)
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  • Registered Nurse RN Clinical Research…

    Banner Health (Sun City, AZ)
    …through interactions with research staff, internal and external investigators, study sponsors and Institutional Review Board ( IRB ). 8. Participates in ... a safe and ethical manner, while ensuring compliance to the FDA and institutional regulations. **Schedule** : Monday - Friday 8am-5pm, This position will primarily… more
    Banner Health (07/10/25)
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  • Heart Institute Clinical Research Data…

    Cedars-Sinai (Los Angeles, CA)
    …and local agencies, including the Food and Drug Administration (FDA) and local Institutional Review Board . Primary Duties and Responsibilities: + ... to be a part of breakthrough research?** The Clinical Research Data Specialist II independently manages data for assigned research studies, demonstrating a high… more
    Cedars-Sinai (07/10/25)
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  • Program Specialist - Training…

    Kennedy Krieger Institute (Baltimore, MD)
    …bibliography and reference pages, and editing and formatting documents. 14. Assist with Institutional Review Board ( IRB ) applications and renewals, ... **Overview** The Program Specialist I provides day-to-day support to team members throughout the planning, implementation, and delivery of Project ECHO (Extension… more
    Kennedy Krieger Institute (07/29/25)
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  • Clinical Research Data Specialist I…

    Cedars-Sinai (Los Angeles, CA)
    …and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board . **ESSENTIAL JOB DUTIES AND RESPONSIBILITIES:** ... and teamwork. Research | Cedars-Sinai The Clinical Research Data Specialist I manages the data for assigned research studies....including the Food and Drug Administration (FDA) and local Institutional Review Board . Maintains research… more
    Cedars-Sinai (07/13/25)
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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. + ... and performance. Manages regulatory paperwork in accordance with human subject IRB , continuing education, clinical trial, and grant agency requirements and… more
    University of Rochester (07/19/25)
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  • Human Subject Research Specialist

    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 (07/03/25)
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  • Clinical Research Coordinator I - Department…

    Cedars-Sinai (Los Angeles, CA)
    …and study conduct. + Works closely with a regulatory coordinator or directly with the Institutional Review Board ( IRB ) to submit Adverse Events, Serious ... Role** This position will support Dr. Nasima Diana Shadbehr, board -certified neurologist and headache specialist leading the...including the Food and Drug Administration (FDA and local Institutional Review Board . **_*This position… more
    Cedars-Sinai (07/23/25)
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  • Clinical Research Data Specialist II…

    Cedars-Sinai (Los Angeles, CA)
    …and local agencies, including the Food and Drug Administration (FDA) and local Institutional Review Board . **Primary Duties and Responsibilities:** + ... in health and disease. **About the Role** The Clinical Research Data Specialist II independently manages data for assigned research studies, demonstrating a high… more
    Cedars-Sinai (07/30/25)
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