Description
Synterex is hiring a Senior Medical Writer for a fully remote role, with on-site client meetings as requested. The position leads the planning, preparation, coordination, and quality review of clinical regulatory documents such as protocols, study reports, investigator brochures, narratives, and module documents across drug development. The role requires at least five years of medical writing experience in the CRO, biotech, or pharmaceutical field, a bachelor’s degree or higher, and familiarity with clinical and regulatory document requirements, Microsoft applications, document management systems, and collaborative authoring tools.

