PharmD Program Associate - Clinical Operations & Program Management

Regeneron’s PharmD Program is an intensive, interdisciplinary 24-month rotational experience for graduating PharmD and/or PhD candidates. Participants receive training from Regeneron mentors and lead projects in various global development roles, gaining both technical and non-technical skills through diverse training, cross-functional experiences, and ongoing mentorship.

About the role

This 2-year development program exposes candidates to critical issues and decision-making processes, high-level business and department operations, and hands-on work experience across different areas. The program is based in Tarrytown, NY, with up to 15% travel required.

Program Tracks

Associates will complete a 24-month rotational experience within one of the following tracks, with opportunities for an optional elective rotation in a different functional area:

• Clinical Operations & Program Management – Support clinical trial management, including trial set-up, execution, conduct, and close-out. In program management, participate in strategic decision-making, governance interactions, and integrated drug development planning.
• Clinical Sciences
• Regulatory Strategy
• Regulatory Labeling & Advertising/Promotion
• Safety Sciences

Responsibilities

• Draft documents integral to clinical sites and regulatory submissions
• Analyze data from clinical studies in preparation 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 the safety profile of products throughout their development lifecycle
• Work with program mentors to improve skills and reach professional goals
• 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
• 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 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, 401(k) company match
• Health and wellness programs, 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 (for jobs in Canada). The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may influence certain elements of pay or benefits.

Schedule

This is a 2-year rotational program. Many roles require on-site performance; please discuss expectations with your recruiter and hiring manager.