Lead clinical medical writing remotely from Ontario, applying regulatory expertise and scientific communication skills to complex study deliverables. Collaborate across Syneos Health teams.As a Senior Medical Writer, you will manage writing activities for individual studies with minimal supervision. You will prepare clinical documents, review statistical outputs, and coordinate comments across departments. The work supports biopharmaceutical, device, and contract research organization projects.Key Responsibilities:Lead transparent, accurate medical writing deliverables and resolve client commentsPrepare protocols, clinical study reports, narratives, and regulatory submissionsCoordinate quality, editorial, source documentation, and team reviewsReview statistical plans and table, figure,



listing specificationsMentor writers and provide technical support, training, and consultationRequirements:Three to five years of relevant medical, technical, or scientific writingBiopharmaceutical, device, or contract research organization industry experienceStrong understanding of FDA and ICH regulationsExtensive English grammar and transparent communication skillsStrong familiarity with AMA Manual of StyleBring senior medical writing, regulatory knowledge, and scientific review expertise to Syneos Health's remote Ontario team.

📌 Senior Clinical Medical Writer (Quebec City)
🏢 Syneos Health
📍 Quebec City