Associate Director, Program Management
Bristol Myers Squibb
September 12, 2026
Full-time
Remote friendly (San Diego, CA)
Worldwide
Operations
Role: Associate Director of Program Management responsible for cross-functional planning and execution of biopharma development programs. Objectives include defining development strategy, managing timelines, and mitigating risks in radiopharmaceutical therapies. Responsibilities encompass building integrated project plans, identifying dependencies, challenging assumptions, facilitating team communication, and implementing best practices for efficient drug development. Qualifications require a BA/BS with 5+ years in biotech or pharma, with drug development experience from pre-IND to NDA, and prior project management expertise. Preferred credentials include an advanced degree (MS, PhD, MBA) and PMP certification. High-value specifics involve clinical-stage programs in oncology, particularly radiopharmaceuticals, with emphasis on strategic planning, risk management, and cross-functional leadership. The role requires collaboration with multidisciplinary teams and involves working in a hybrid San Diego environment, with no travel specified.