Associate Director, Global Regulatory Strategy (Heme/Onc)

Bristol-Myers Squibb is looking for an Associate Director in Princeton, NJ to lead regulatory dossier submissions and develop strategies for global regulatory compliance. The ideal candidate has a strong background in regulatory affairs and significant experience with FDA submissions.

Key responsibilities include managing cross-functional teams and ensuring compliance with drug development processes. Applicants should have a PhD, MD, or equivalent, and experience in the pharmaceutical industry.