The Director, IRB Operations, reports to the Director, Human Research Protection Program (HRPP). This position is responsible for administrative oversight for all operations supporting the functions of the BIDMC Committee for Clinical Investigations-Institutional Review Board (CCI-IRB). The primary areas of responsibility are 1) management of CCI-IRB staff, including IRB Manager and Reliance Manager, 2) serving as the administrative interface between the Chair and other Vice-chairs and the CCI-IRB staff and the clinical research community, and 3) serving as the primary regulatory/ethical resource for CCI committee members, researchers, and research coordinators on humans subject protection, and 4) works with the Director of the Human Research Protection Program for the development, implementation and management of Institutional Review Board policies and procedures and the related administrative operations of CCI protocol office in order to comply with all federal and state regulations; 5) making determinations of research engagement / human subjects research; 6) work with BILH legal and Sponsors to revise consent language where changes are requested to the template language.
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Job Type
Full-time
Career Level
Director