PharmD Program Associate - Regulatory Labeling & Advertising/Promotion

Regeneron’s PharmD Program is an intensive, interdisciplinary program for graduating PharmD and/or PhD candidates. It combines training by Regeneron mentors with hands-on experience leading projects in various global development roles, providing depth and breadth within the Global Development organization. Participants develop technical and non-technical skills through diverse training, cross-functional experiences, and ongoing mentorship.

About the Program

This 2-year development program offers rotational assignments exposing candidates to critical issues, decision-making processes, high-level business knowledge, and hands-on experience in different areas. Associates may also gain exposure to a different functional area through an optional elective rotation.

Location & Travel

Primary location: Tarrytown, NY. Travel may be up to 15%.

Program Tracks

The program includes a 24-month rotational experience within one of the following tracks:

• Clinical Operations & Program Management
• Clinical Sciences
• Regulatory Strategy
• Regulatory Labeling & Advertising/Promotion – Associates contribute to labeling content and strategies, interpret regulations and guidelines, support the labeling process throughout the product lifecycle, and ensure promotional communications comply with FDA regulations. They also advise teams on regulatory risks and support interactions with the FDA-Office of Prescription Drug Promotion (OPDP).
• Safety Sciences

Responsibilities

• Draft documents integral to clinical sites and regulatory submissions.
• Analyze data from clinical studies for interactions with ethics committees, senior management, regulatory authorities, and others.
• Manage third-party vendors and maintain timelines of key results.
• Develop regulatory strategies for clinical development programs.
• Analyze safety data to characterize product safety profiles throughout their development lifecycle.
• Work with program mentors to improve professional skills.
• 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 in a life science-related field may also be considered.
• Degree must be completed 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 with a desire to build a career 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:

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

For additional details on U.S. benefits, visit Regeneron Total Rewards. For other locations, information will be provided during the recruitment process.

Pay

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

Schedule

Many roles are required to be performed on-site. On-site expectations for this role and location will be discussed during the recruitment process.