PharmD Program Associate - Safety Sciences at Regeneron
Tarrytown, New York, USA -
Full Time


Start Date

Immediate

Expiry Date

08 Dec, 25

Salary

96700.0

Posted On

08 Sep, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Preparation, Third Party Vendors, Development Programs, Timelines, Regulatory Submissions

Industry

Pharmaceuticals

Description

The PharmD Program is an intensive, interdisciplinary program for graduating PharmD 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.
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.

IN THIS PROGRAM, YOU MAY EXPERIENCE:

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

Responsibilities

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 science-minded, ask questions, and advocate for your ideas
You work with precision, intellect, and integrity
You are ready to work with a team that can bring great ideas to life and make a difference in the healthcare industry
To be considered for this role, you must have completed your PharmD degree by Summer 2026. Industry or research experience is preferred. You are comfortable with up to 15% travel and are eligible to work in the U.S. on a permanent basis. A PhD in a related scientific filed may also be considered.

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