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tracks adverse events (AE). Reports serious AEs to IRB and sponsor. Documents all protocol deviations, reconciles test article accountability at study close out and prepares summary report for
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availability. Reports and tracks adverse events (AE). Reports serious AEs to IRB and sponsor. Documents all protocol deviations, reconciles test article accountability at study close out and prepares
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. Reports and tracks adverse events (AE). Reports serious AEs to IRB and sponsor. Documents all protocol deviations, reconciles test article accountability at study close out and prepares summary report
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University of North Carolina at Chapel Hill | North Wilkesboro, North Carolina | United States | about 1 month ago
required for IRB initial and continuing review ( IRB application, consent & HIPPA forms). The CRA will prepare and submit regulatory documents as required by trial sponsor. This position requires on-site
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management tasks. The position also supports Institutional Review Board (IRB) submissions, participant compensation processes, and the development and dissemination of research and educational
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. The link to our website is: https://www.uab.edu/onealcancercenter/ Please attach a current resume with this application. General Responsibilities To serve as primary coordinator for clinical
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comprehensive regulatory management of clinical research studies, ensuring compliance with FDA , IRB , institutional, sponsor, and consortium requirements from study start-up through closeout. Key
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data. Assist with Institutional Review Board (IRB) filings and inquiries, and assist in the preparation of manuscripts, grant proposals, and research related presentations. Works closely with the
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data. Assist with Institutional Review Board (IRB) filings and inquiries, and assist in the preparation of manuscripts, grant proposals, and research related presentations. Works closely with the
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Posting Details I. DEPARTMENT INFORMATION Job Description Summary: The Research Associate is expected to have some experience in clinical research: submitting IRB protocols and consent forms