PharmD Program Associate - Safety Sciences

Role: The program is a 2-year rotational development initiative for recent PharmD and PhD graduates focusing on Global Development roles, with tracks in Clinical Operations & Program Management, Clinical Sciences, Regulatory Strategy, Regulatory Labeling & Advertising/Promotion, and Safety Sciences. Objectives include gaining comprehensive experience across clinical, regulatory, safety, and operational functions within the biopharma industry. Responsibilities: involve drafting regulatory documents, analyzing clinical data, managing vendors, developing clinical strategies, assessing product safety profiles, and engaging in cross-functional projects. Requirements: PharmD or PhD degree by Summer 2027, with prior internship or industry experience preferred; familiarity with clinical trial evaluation and data analysis; U.S. work eligibility; highly motivated with career interests in clinical sciences, regulatory affairs, or safety sciences. Preferred: post-doctoral training in life sciences. HighValue: pharmacovigilance with focus on signal detection, clinical development, regulatory strategy, global clinical operations, and cross-functional collaboration. WorkSetup: Tarrytown, NY, with up to 15% travel.