PharmD Program Associate - Safety Sciences

The PharmD Program is an intensive, interdisciplinary program for graduating PharmD and/or PhD candidates. It consists of training by Regeneron mentors and experience leading projects in various global development roles, providing participants depth and breadth of experience within Regeneron's Global Development organization. Associates will acquire technical and non-technical skills through diverse training, cross-functional experiences, and ongoing mentorship.

About the role

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

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
• Safety Sciences

Associates will also have opportunities to gain exposure to a different functional area through an optional elective rotation. In the Safety Sciences track, Associates will gain working knowledge of pharmacovigilance (PV) disciplines, focusing on signal detection and management, case processing operations, and PV business support functions.

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 and 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
• Degree completion required 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, 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

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

Pay

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

Many roles are required to be performed on-site. Background checks may be conducted in accordance with applicable laws.