PharmD Program Associate - Regulatory Strategy

Role: The program offers a 24-month rotational experience for PharmD and PhD candidates, focused on global development functions within biopharma, including Regulatory Strategy. Objectives include developing technical and leadership skills, gaining broad exposure to drug development processes, and supporting regulatory planning and submissions. Responsibilities encompass drafting clinical and regulatory documents, analyzing clinical data, managing third-party vendors, developing regulatory strategies, and assessing product safety profiles. The program provides cross-functional training through rotations in Clinical Operations, Clinical Sciences, Regulatory Strategy, Labeling & Promotion, and Safety Sciences, with optional electives. Requirements: Post-doctoral degree (PharmD or PhD) from an accredited institution by Summer 2027; exposure to clinical trial data, literature, or biotech/pharma internships preferred; U.S. work eligibility; motivated to build a career in clinical sciences, regulatory affairs, or safety sciences. HighValue: Focus on pharmaceutical development, regulatory planning, clinical data analysis, with opportunities for global engagement and site visits. Work setup: located in Tarrytown, NY, with up to 15% travel.