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 clear, accurate medical writing deliverables and resolve client comments
Prepare protocols, clinical study reports, narratives, and regulatory submissions
Coordinate quality, editorial, source documentation, and team reviews
Review statistical plans and table, figure,



listing specifications
Mentor writers and provide technical support, training, and consultation
Requirements: Three to five years of relevant medical, technical, or scientific writing
Biopharmaceutical, device, or contract research organization industry experience
Strong understanding of FDA and ICH regulations
Extensive English grammar and explicit communication skills
Strong familiarity with AMA Manual of Style
Bring senior medical writing, regulatory knowledge, and scientific review expertise to Syneos Health’s remote Ontario team.

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