Executive Director, Head of Clinical Design & Delivery Center

Role: Executive Director, Clinical Design and Delivery Center (CDDC), overseeing the Protocol Management Office (PMO) to ensure high-quality review of clinical protocols, SAPs, and DMC charters across BMS's therapeutic portfolio. Responsibilities include leading scientific review processes, developing and refining protocol review systems, and driving continuous improvement through metrics and industry insights. The role also involves designing and delivering educational programs to enhance clinical development capabilities, fostering innovation and efficiency initiatives, and integrating advanced technology like AI to optimize trial design and reduce operational burdens. Additionally, the role serves as a strategic leader in advancing clinical process excellence, aligning with regulatory and compliance standards, and representing BMS externally in industry forums. Requirements: PhD, MD, PharmD, or equivalent in Life Sciences; at least 10 years in clinical development with extensive experience in protocol design, review, and regulatory compliance; proven leadership in complex global matrices; expertise in early to late-stage drug development. Preferred skills include deep knowledge of GxP, clinical operations, statistics, epidemiology, and experience with digital innovation and real-world evidence integration. High-value: involvement in multi-therapeutic areas, cross-functional leadership, strategic innovation, and technology deployment. Work setup: not specified.