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Senior Medical Writer, Safety Support Services

Merck • Bogota, NJ, US • published 2026-10-23 14:05:16.892157

Description

Job Description The Clinical and Regulatory Strategic Communications (CRSC) department within 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 Senior Medical Writer, in partnership with a project lead, develops, authors, edits and leads 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. **The Senior Medical Writer:** * 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\...

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