• 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 ...job (OTJ) training. OTJ training includes two years of Institutional Review Board ( IRB more
    Sanford Health (05/30/25)
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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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  • 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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  • 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 ... records and spreadsheets related to the job functions. + Review batch records and release products. Revise/ review ...as deemed necessary. + Manage documentation associated with all IRB activities related to sponsor and study site submissions… more
    Charles River Laboratories (05/14/25)
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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 (03/26/25)
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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 , ... assist the regulatory specialist in preparing for all local and Central Institutional Review Board ( IRB ) documentation through the IRB , including… more
    University of Pennsylvania (05/04/25)
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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 (04/11/25)
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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 (04/26/25)
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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 (04/16/25)
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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 (06/14/25)
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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 ... the following duties: o Knowledge of all regulatory requirements and institutional requirements when conducting the study protocol(s). o Participant recruitment… more
    Dignity Health (06/07/25)
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  • Research Regulatory Specialist

    BayCare Health System (Clearwater, FL)
    …and laws. + Acts as a liaison between the sponsor, Clinical Research Operations, Institutional Review Board and internal departments/ staff to complete ... initial Institutional Review Board protocol submissions. + Submit study amendments in a timely fashion including changes to the protocol, consent forms and… more
    BayCare Health System (06/17/25)
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  • Research Revenue Cycle Compliance…

    AdventHealth (Orlando, FL)
    …or in research administration such as a centralized research office, or with an institutional review board + Experienced in medical billing, medical coding, ... **The role you'll contribute:** The Research Revenue Cycle Compliance Specialist performs duties in support of the Research Billing...such as a centralized research office, or with an institutional review board . + Experience… more
    AdventHealth (06/14/25)
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  • Human Subject Research Specialist I

    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 (06/06/25)
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  • Human Subject Research Specialist I

    University of Rochester (Rochester, NY)
    …with study families, and document adverse events and report to senior study staff, PI, Institutional Review Board ( IRB ), Sponsor, and/or any other ... by the PI, and ensures consent forms are complete, accurate, and available for review . Prepares documents for data uploads to NIMH Data Archive (NDA) system and… more
    University of Rochester (04/07/25)
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  • Clinical Research Regulatory Specialist

    Baylor Scott & White Health (Dallas, TX)
    …before submission. Follow up, communicate, and facilitate responses to queries from the IRB , Sponsor, and other committees after their review . + Coordinates the ... University Medical Center.** **Job Summary** The Clinical Research Regulatory Specialist supports clinical research by developing protocol-specific documents and… more
    Baylor Scott & White Health (06/20/25)
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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 (04/24/25)
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  • Clinical Research Data Specialist I - Per…

    Cedars-Sinai (Los Angeles, CA)
    …and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board . Primary Duties and Responsibilities: + Manages ... team is seeking a highly motivated Clinical Research Data Specialist I to join their team. Heart | Cedars-Sinai...**Summary of Essential Job Duties:** The Clinical Research Data Specialist I manages the data for assigned research studies.… more
    Cedars-Sinai (05/07/25)
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  • Research Grant Specialist III - Women's…

    Cedars-Sinai (CA)
    …Health (NIH), Department of Defense (DOD), Food and Drug Administration (FDA) and the Institutional Review Board . Prepares and routes internal documents for ... Description** **Grow your career at Cedars-Sinai!** The Research Grants Specialist III ('RGS III') plays a vital role in...**Req ID** : 8612 **Working Title** : Research Grant Specialist III - Women's & Guerin Children's (Full-Time, Hybrid)… more
    Cedars-Sinai (05/02/25)
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  • Clinical Nurse Specialist RN

    AdventHealth (Orlando, FL)
    …nurses who are involved in developing research projects/protocols. Participates with the Institutional Review Board and Nursing Research Council. **The ... registered professional nurse + Current registration with Florida State Board of Nursing as a Clinical Nurse Specialist... Board of Nursing as a Clinical Nurse Specialist + Basic Life Support (BLS) certification + Advanced… more
    AdventHealth (03/26/25)
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