PharmD Program Associate - Clinical Operations & Program Management

Regeneron; Village of Tarrytown (NY); On-site; USD 90,000 - 120,000; Full time

Job summary

Regeneron invites graduates to join the PharmD Program in Tarrytown, NY, a two-year interdisciplinary development track designed to build expertise in global development roles.

Participants rotate through Clinical Operations, Regulatory Strategy, Safety Sciences and more, gaining hands-on experience, mentorship, and exposure to decision-making processes across programs. The program emphasizes cross-functional training and site-based activities.

Qualifications

• Post-doctoral graduates from an ACPE PharmD program or PhD in life sciences by Summer 2027.
• Internship or rotational pharma/biotech exposure is a plus.
• Ability to work in the U.S. on a permanent basis.

Responsibilities

• Drafting documents integral to clinical sites and regulatory submissions.
• Analyzing data from clinical studies for ethics committee and regulatory interactions.
• Managing third-party vendors and maintaining timelines of key results.
• Developing regulatory strategies for clinical development programs.
• Analyzing safety data to characterize product safety across development.
• Learning from mentors to improve professional skills and goals.
• Opportunities to travel to clinical sites or health authority meetings.

Education

PharmD or PhD in life sciences

Job description

Build our future together:

The PharmD Program is an intensive, interdisciplinary program for graduating PharmD and/or PhD candidates. The program consists of training by Regeneron mentors and experience leading projects in various global development roles.

This unique program provides participants depth and breadth of experience within Regeneron's Global Development organization. Participants will acquire technical and non-technical skills throughout the program through diverse training, cross-functional experiences, and ongoing mentorship. Assignments in this 2-year development program will expose candidates to critical issues and decision-making processes, acquire high-level knowledge of the business and department operations, and gain hands-on work experience in different areas.

When & where:

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
• Regulatory Labeling & Advertising/Promotion
• Safety Sciences

Associates will also have opportunities to gain exposure to a different functional area through an optional elective rotation as a part of the 24-month program.

Clinical Operations & Program Management

Associates will support the management of clinical trials by actively contributing to key activities related to trial set-up, execution, conduct and close out. In program management, the Associates will broaden their scope and participate in activities related to strategic decision making, governance interactions and integrated drug development planning.

Discover your role:

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

This role requires:

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

Application Dates

Applications Accepted: August 24th, 2026 - September 11th, 2026

We are committed to building a workplace with an inclusive culture.

Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

Where necessary, we disclose salary ranges for roles in all countries in which we operate. 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 apply and influence certain elements of pay or 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, dent