Director IRB Ops

The Director of IRB Operations provides administrative oversight for the BIDMC Committee for Clinical Investigations-Institutional Review Board, managing staff and serving as the primary regulatory and ethical resource for the clinical research community. This role involves developing IRB policies, determining research engagement protocols, and ensuring compliance with federal and state regulations regarding human subject protection. The position requires coordinating schedules for board members and leading the development of training materials to maintain adherence to institutional and external guidelines.