PharmD Program Associate - Clinical Sciences

Role: The program offers a 24-month interdisciplinary rotational experience for recent PharmD and PhD graduates, focusing on Clinical Sciences within biopharma drug development. Objectives include gaining comprehensive exposure to clinical trial management, regulatory strategies, safety data analysis, and cross-functional collaboration across global development teams. Responsibilities involve drafting regulatory documents, analyzing clinical data, managing vendors, developing clinical development strategies, and supporting interactions with ethics committees and health authorities. Requirements: PharmD or PhD in life sciences by Summer 2027, post-doctoral or industry internship experience preferred, familiarity with clinical trial evaluation, motivated to build a career in clinical sciences, regulatory, or safety sciences; eligible to work in the U.S. Candidates must have completed their degree by Summer 2027. Preferred qualifications include prior industry rotational experience. High-Value: Focus on clinical sciences in drug development, working on early to late-phase trials (pre-IND through pivotal trials), exposure to regulatory strategy and safety profiling, with up to 15% travel. Location: Tarrytown, NY, with onsite work required. The program provides cross-functional mentorship and optional elective rotations across development tracks including Clinical Operations, Regulatory Strategy, and Safety Sciences.