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Senior Nonclinical Medical Writer: Regulatory Submissions Lead
Job in
South San Francisco, San Mateo County, California, 94083, USA
Listed on 2026-09-03
Listing for:
Merck & Co.
Full Time
position Listed on 2026-09-03
Job specializations:
-
Research/Development
Regulatory Compliance Specialist
Job Description & How to Apply Below
Merck & Co. is seeking an experienced Medical Writer to join the Nonclinical Pharmacology Documentation group. The role focuses on generating preclinical reports and submission modules to support development programs, with collaboration across research and regulatory functions.
The successful candidate will manage multiple programs, prioritize timelines, and ensure high-quality regulatory documents for CTD, IND, NDA/BLA/MAA submissions, while contributing to templates and adopting new AI tools.
#J-18808-LjbffrPosition Requirements
10+ Years
work experience
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