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IRB Administrator, Clinical Trials Specialist
This position is responsible for conducting pre- and post-reviews of FDA-regulated and clinical trial research, identifying and documenting deficiencies or missing materials, communicating outcomes or clarification requirements with researchers and study staff, assessing readiness of submissions and re-submissions for IRB review. This role will be a subject matter expert for Institutional Review Board (IRB) members, faculty, staff, students, and other researchers for FDA-regulated and clinical trial review requirements, securing authoritative reference materials, communicating with regulatory agencies, identifying and analyzing emerging regulatory developments and trends, and developing resource materials for distribution/disse


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