Associate Director, Regulatory Affairs

📋 Description

• • As an Associate Director in Regulatory Affairs at RayzeBio, a wholly-owned subsidiary of Bristol Myers Squibb, you will serve as a Global Regulatory Lead for cutting-edge radiopharmaceutical programs, driving regulatory strategy for oncology therapeutics and diagnostics to advance transformative cancer treatments.
• • You will author regulatory documents, lead preparation and submission of global filings (IND, CTA/IMPD, marketing applications), and represent the company in interactions with regulatory authorities such as the FDA and EMA, ensuring compliance and strategic alignment across clinical and nonclinical development.
• • RayzeBio combines the agility of an emerging biotech with the global resources of BMS, focusing on targeted radioisotope therapies for solid tumors, and operates as a mission-driven, multidisciplinary team where innovation and patient impact are central to daily work.
• • In this role, you will deepen your expertise in radiopharmaceutical regulatory landscapes, lead cross-functional teams, influence global regulatory strategy, and contribute directly to the development of life-saving cancer therapies while growing as a strategic leader in a high-impact biotech environment.