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Job Description
PharmD Program Associate – Clinical Operations & Program Management | Regeneron
The Tone:
This is a full-time, 2-year rotational development program at Regeneron, located in Tarrytown, NY, with potential for up to 15% travel. Regeneron is a leading biotechnology company focused on inventing and developing life-transforming medicines. This PharmD Program offers graduating PharmD and/or PhD candidates an intensive, interdisciplinary experience within the Global Development organization, providing both depth and breadth of exposure through training by Regeneron mentors and leadership opportunities on key projects. Participants will acquire vital technical and non-technical skills, gaining hands-on work experience in different areas and a high-level understanding of business and department operations.
The TL;DR
• Role: Internship
• Type: Full-time
• Location: In-person, Tarrytown, NY
• Pay: $98100–$160100 yearly
• Team: Global Development organization, specifically within the Clinical Operations & Program Management track.
• Mission: Support the management of clinical trials and participate in strategic drug development planning to advance Regeneron’s pipeline.
What You’ll Actually Do
• Manage: Contribute to the management of clinical trials through all phases from set-up, execution, conduct, and close-out.
• Draft: Prepare essential documents integral to clinical sites and regulatory submissions.
• Analyze: Evaluate clinical study data in preparation for interactions with ethics committees, senior management, and regulatory authorities.
• Oversee: Manage third-party vendors and maintain critical timelines for key project results.
• Strategize: Participate in strategic decision-making, governance interactions, and integrated drug development planning activities.
The Must-Haves
• Background: Doctorate Degree. Entry-Level. Post-doctoral graduates from an accredited (ACPE) College of Pharmacy program (PharmD) or PhD graduates within a life science related area of study are required. Degree must be completed by Summer 2027.
• Experience: Exposure or familiarity with evaluating clinical trials, scientific literature, and data analysis is expected. Candidates will be provided with hands-on work experience in different areas of global development.
• Skills: Strong analytical capabilities for evaluating clinical trials, scientific literature, and various datasets. Foundational understanding or strong interest in clinical sciences, global clinical operations, regulatory affairs, and/or safety sciences is essential for building a career within the program. Eligibility to work in the U.S. on a permanent basis is also required.
• Bonus: Prior internship or rotational experience within the Pharmaceutical/Biotech industry is a plus.