About this role
Associate Director, Commercial Regulatory Affairs at Bristol Myers Squibb. Location: Princeton, New Jersey, United States. Role: providing advice, assessing risk, leading training Requirements: BS required; 3+ years regulatory promotional review or 5+ years pharmaceutical experience; ability to provide regulatory advice, risk assessment, and work with OPDP; strong communication and analytical skills. Category: Legal and Compliance Seniority: Mid Level Commitment: Full Time Workplace: Onsite Languages: English