Associate Director, Program Management
Bristol Myers Squibb
September 15, 2026
Full-time
Remote friendly (San Diego, CA)
Worldwide
Operations
Role: Associate Director of Program Management responsible for cross-functional planning and execution of development programs at RayzeBio, a biopharma specializing in radiopharmaceuticals for oncology. Responsibilities: develop and maintain integrated program plans, manage timelines, identify risks, develop mitigation strategies, and drive strategic execution to ensure timely, on-budget delivery. Collaborate closely with clinical development teams, regulatory, and project stakeholders; oversee risk management and communication across teams; implement best practices and process improvements. Requirements: BA/BS with 5+ years in biotech or pharma, with clinical-stage drug development experience (pre-IND through NDA), preferably in oncology or radiopharmaceuticals. Experience managing global regulatory submissions (INDs/NDAs) and familiarity with project management tools such as Microsoft Office and Smartsheet. Preferred: advanced degree (MS, PhD, MBA), PMP certification, and experience applying AI tools for decision-making. High-Value: drug development focus on radiopharmaceuticals in oncology, at various stages from preclinical to clinical, with regulatory and cross-functional leadership. Work setup: based in San Diego, CA, with a focus on remote/hybrid work and collaboration with global teams.