Principal Medical Writer

MSD • North Wales, PA, US • published 2026-09-21 22:42:50.121790

Description

Job Description The Clinical and Regulatory Strategic Communications (CRSC) department within Global Clinical Trial Operations (GCTO) creates and delivers high\-quality regulated content in support of our development pipeline and enables data sharing for our customers. We are a strategic partner that ensures excellence and compliance with applicable laws while incorporating health literacy principles in the development of public\-facing materials. The Principal Medical Writer, in partnership with a project lead, leverages strategic and scientific expertise to develop, author, edit, and lead the review of accurate, clear, and compliant clinical, regulatory, and/or public‑facing documents, across multiple programs and therapeutic areas, in support of the company portfolio. **In this role, the Principal Medical Writer:** * Is recognized as a subject matter expert in the design, planning, authoring, editing, and review of accurate, clear, high\-quality documents that reflect applicable medical writing best practices (e.g., lean writing, health literacy) and evolving regulatory requirements * Is recognized as a strong scientific contributor and collaborator on cross\-functional teams an...

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