PharmD Program Associate - Regulatory Strategy

Build our future together:   The PharmD Program is an intensive, interdisciplinary program for graduating PharmD and/or PhD candidates. The program consists of training by Regeneron mentors and experience leading projects in various global development roles.   This unique program provides participants depth and breadth of experience within Regeneron's Global Development organization. Participants will acquire technical and non-technical skills throughout the program through diverse training, cross-functional experiences, and ongoing mentorship. Assignments in this 2-year development program will expose candidates to critical issues and decision-making processes, acquire high-level knowledge of the business and department operations, and gain hands-on work experience in different areas.     When & where:   Location: Tarrytown, NY   Travel percentage: Up to 15%     Program Tracks:   The program is comprised of a 24-month rotational experience within one of the following tracks:   Clinical Operations & Program Management   Clinical Sciences  Regulatory Strategy   Regulatory Labeling & Advertising/Promotion   Safety Sciences     Associates will also have opportunities to gain exposure to a different functional area through an optional elective rotation as a part of the 24-month program.     Regulatory Strategy – The regulatory associate will support global regulatory planning and execution to support the clinical development, approval, and lifecycle management of pharmaceutical products. This position partners cross-functionality to define innovative regulatory pathways, ensure compliance with global health authority requirements and guidances, and produce and manage timelines and deliverables across multiple programs. The associate will provide strategic input on operations and submissions to global regulatory authorities to enable efficient and successful product development.   Discover your role:   Drafting documents integral to clinical sites and regulatory submissions   Analyzing data from clinical studies in preparation for interactions with ethics committees, senior management, regulatory authorities, and others   Managing third-party vendors and maintaining timelines of key results   Developing regulatory strategies for clinical development programs   Analyzing safety data to characterize the safety profile of products throughout their development lifecycle   Working with program mentors to improve skills to reach professional goals better   Opportunities to travel to clinical sites and/or meetings with health authorities     This role requires:   Post-doctoral graduates from an accredited (ACPE) College of Pharmacy program (PharmD); PhD graduates within a life science related area of study may also be considered.   You must have completed your PharmD and/or PhD degree by Summer 2027   Prior Internship or rotational experience within the Pharmaceutical/Biotech industry a plus   Exposure or familiarity with evaluating clinical trials, scientific literature and data    You are highly motivated and seek to build a career with a foundation in Clinical Sciences, Global Clinical Operations, Regulatory Affairs, and/or Safety Sciences   You are eligible to work in the U.S. on a permanent basis     Application Details:   When applying, please include a resume and cover letter specifying the track you are interested in. If you are interested in more than one track, please rank them in order of preference.     Applications Accepted: August 24th, 2026 - September 11th, 2026   For more information on the tracks, program, and interview process, please refer to the brochure.   Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all  qualified applicants will receive consideration for employment without regard to race, color, religion or