PharmD Program Associate - Regulatory Labeling & Advertising/Promotion

Role: Participate in Regeneron's 2-year interdisciplinary PharmD/PhD program focused on clinical sciences, regulatory strategy, or safety sciences, with rotational experiences in global development functions. Responsibilities: contribute to regulatory labeling strategies, draft documents for clinical sites and submissions, analyze clinical trial data, manage vendors, develop regulatory strategies, and interpret safety data throughout product lifecycle. Requirements: PharmD or PhD in life sciences, completed by Summer 2027; prior internship or industry experience preferred; familiarity with clinical trial data and regulatory guidelines; U.S. work eligibility. HighValue: program involves cross-functional training, exposure to clinical development, regulatory affairs, and safety sciences; includes optional rotations and up to 15% travel; located in Tarrytown, NY.