When & where:
Program Tracks:
The program is comprised of a 24-month rotational experience within one of the following tracks:
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.
Regulatory Labeling & Advertising/Promotion 6 Associate will contribute to the development of labeling content and labeling strategies through interpretation of regulations and guidelines; and support the labeling process throughout the product lifecycle, including Labeling Working Group reviews and management approvals. The associate will also develop knowledge and skills to interpret FDA regulations and guidances to ensure promotional communications are truthful and not misleading, and appropriately advise teams on associated regulatory risks, and support FDA-Office of Prescription Drug Promotion (OPDP) interactions.
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 SciencesYou are eligible to work in the U.S. on a permanent basis
Application Details:
When applying, please include a resume and cover letter specifying the track you are interested in. If you are interested in more than one track, please rank them in order of preference.
Applications Accepted: August 24th, 2026 - September 11th, 2026
For more information on the tracks, program, and interview process, please refer to the brochure.
Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed onsite. Please speak with your recruiter and hiring manager for more information about onsite expectations for your role and location.
As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.
For jobs in Canada: this posting is for an existing position.
Salary Range (annually)
$98,100.00 - $160,100.00
