PharmD Program Associate - Clinical Operations & Program Management

Role: The PharmD Program is a 2-year interdisciplinary development initiative for recent PharmD and PhD graduates, focusing on global clinical development functions within Regeneron. Objectives include gaining comprehensive experience across clinical operations, scientific research, regulatory strategy, safety sciences, and related areas through rotational assignments and mentorship. Responsibilities involve supporting clinical trial management—drafting key documents, analyzing clinical data, managing vendors, developing regulatory strategies, and safety profiling—alongside participation in strategic decision-making and cross-functional projects. Qualifications: Post-doctoral degree (PharmD or PhD in life sciences) completed by Summer 2027; prior industry internship or rotational experience preferred; familiarity with clinical trial evaluation and data analysis; U.S. work eligibility. Preferred skills include motivation for careers in clinical sciences, regulatory affairs, or safety sciences. High-Value: Focus on clinical trial processes, regulatory strategy, safety profiling, and cross-functional exposure; location in Tarrytown, NY, with up to 15% travel. Work setup: on-site with rotational and optional elective experiences.