• 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 ... study personnel. + Acts as a liaison between the institutional review committees, regulatory agencies, and the...+ Assists in the preparation of research protocols for IRB submission, submitting protocol amendments, preparing renewals,… 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 ... 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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  • 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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  • 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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  • 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 (07/24/25)
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  • Regulatory Specialist - CRI

    Methodist Health System (Dallas, TX)
    …the IRB . * Create and/or adapt clinical trial informed consent documents for Institutional Review Board ( IRB ) submission. * Maintain regulatory ... Shift :** **Job Description :** Your Job: The Regulatory Specialist will perform expertise in the regulatory component of...events in accordance with Food and Drug Administration, sponsor protocol , and IRB regulations and guidelines. *… more
    Methodist Health System (08/08/25)
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  • Sr. Compliance Monitoring Specialist

    Johns Hopkins University (Fort Defiance, AZ)
    …and regulations, and institutional policies that must be corrected prior to IRB review . + Determine that appropriate protocol and application-specific ... 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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  • 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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