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 transparent 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.

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