Lead regulatory medical writing for Syneos Health remotely from Canada, emphasizing protocols, protocol amendments, and accurate scientific communication. This sponsor-dedicated Senior Medical Writer role focuses on clinical study protocols and protocol amendments. You will manage writing activities across departments with minimal supervision while completing regulatory documents. The work requires transparent scientific presentation, organized reviews, and collaboration with clinical, statistical, regulatory, and medical affairs colleagues.

Lead clear, accurate medical writing deliverables

Manage study writing activities across departments

Resolve client comments and coordinate document reviews

Apply ICH E3, templates, and regulatory standards

Three to five years of relevant medical writing experience

Ability to review statistical analysis plans

Understanding of regulatory requirements and guidelines

Willingness to travel less than twenty five percent

Use regulatory writing, protocol development, and scientific review expertise to deliver accurate clinical documents for Syneos Health.

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📌 Senior Medical Writer - Regulatory Writing (Montreal)
🏢 Syneos Health
📍 Montreal