PharmD Program Associate - Regulatory Strategy

Regeneron’s PharmD Program is an intensive, interdisciplinary program for graduating PharmD and/or PhD candidates, offering training by Regeneron mentors and leadership experience on global development projects. This 2-year program provides depth and breadth of experience within Regeneron's Global Development organization, equipping participants with technical and non-technical skills through diverse training, cross-functional experiences, and ongoing mentorship.

About the role

Assignments in this rotational development program will expose candidates to critical issues and decision-making processes, high-level knowledge of business and department operations, and hands-on work experience in different areas. Associates will have opportunities to gain exposure to a different functional area through an optional elective rotation.

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 – 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-functionally 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.
• Regulatory Labeling & Advertising/Promotion
• Safety Sciences

Responsibilities

• 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
• Opportunities to travel to clinical sites and/or meetings with health authorities

Requirements

• 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 is a plus
• Exposure or familiarity with evaluating clinical trials, scientific literature, and data
• Highly motivated and seeking to build a career with a foundation in Clinical Sciences, Global Clinical Operations, Regulatory Affairs, and/or Safety Sciences
• Eligible to work in the U.S. on a permanent basis

Benefits

Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role:

• Annual bonuses or other incentive plans
• Equity awards
• Pension or retirement benefits, 401(k) company match
• Health and wellness programs, fitness centers
• Insurance benefits (e.g., medical, dental, vision, life, and disability)
• Paid time off
• Family support benefits

Pay

Salary Range (annually): $98,100.00 - $160,100.00