• 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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  • Senior 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 ... forms and associated documentation + Serves as a liaison between the institutional review committees, regulatory agencies, and the investigators to ensure… more
    Houston Methodist (08/16/25)
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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 ... looking to leverage your abilities - apply today. The **RN Clinical Research Specialist ** at **Banner MD Anderson Cancer Center Clinical** Trials Office plays a… more
    Banner Health (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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  • Clinical Trial Specialist

    Actalent (New Brunswick, NJ)
    …medication diaries, eligibility checklists, and flow sheets. + Verify Scientific Review Board , Institutional Review Board , data collection plans, and ... research team for timely prescreening of potential subjects and review patient charts for protocol eligibility. +...Ensure informed consent is obtained and documented according to IRB , GCP, and institutional policies. + Provide… more
    Actalent (08/12/25)
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  • Research Support Specialist

    Stony Brook University (Stony Brook, NY)
    … documents when required, manage medical charts, and ensure compliance with all Institutional Review Board policies. The successful incumbent must have ... Research Support Specialist **Required qualifications (as evidenced by an attached...research tool. Experience with preparation of regulatory materials (eg, IRB , grant progress reports). Experience with purchasing, and/or budget… more
    Stony Brook University (08/08/25)
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