PharmD Program Associate - Safety Sciences

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.  Safety Sciences – Associate will gain a working knowledge of various pharmacovigilance (PV) disciplines that enable the continuous assessment of the benefit-risk of Regeneron products throughout the product life cycle, from early clinical development through market authorization and including post marketing surveillance, with a focus on signal detection and management. The Associate will build foundational knowledge and experience in case processing operations and will gain an understanding of various PV business support functions enabling a global pharmacovigilance organization, while also having the opportunity to interface cross-functionally on tasks/projects. 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