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Senior Medical Writer, Clinical and Regulatory Strategic Communications (CRSC)

MSD • Rahway, NJ, US • published 2026-10-23 02:05:07.173334

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. * Demonstrates independence in preparing clinical regulatory (e.g., protocols, clinical study reports, participant narratives, investigator’s brochures) and/or public\-facing (e.g., informed consent forms, clinical trial registration and results postings, plain language summaries) documents per company and evolving regulatory requirements. * Applies an in\-depth knowledge and understanding of 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). * Is a scientific contributor and collaborator on document\-specific cross\-functional teams and demonstrates an understanding of team and project leadership respons...

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