Lead regulatory content strategies as a Senior Medical Writer with Amaris Consulting in Mississauga, Ontario. Drive high-quality documentation for global submissions with a hybrid work model.
In this key role, you will develop and execute strategies for regulatory submissions. Bring your expertise in managing clinical dossiers and ensuring compliance with global regulations. Collaborate with cross-functional teams to facilitate effective communication with health authorities and mentor junior writers.
Key Responsibilities:
• Lead regulatory content strategies for global submissions
• Manage clinical dossier preparation and safety documentation
• Develop content plans aligning with project timelines




• Review documents for accuracy and regulatory compliance
• Collaborate to resolve content-related issues and improve standards
Requirements:
• Bachelor’s in Life Sciences or related field
• Minimum 5 years in regulatory or medical writing
• Robust knowledge of ICH, GCP, and GxP regulations
• Proficiency in Google Workspace and Microsoft Office
• Excellent communication and project management skills
Enhance your career by producing impactful regulatory documentation and collaborating on cutting-edge content strategies.
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📌 Senior Medical Writer At Amaris Consulting Mississauga (Canada)
🏢 Amaris Consulting
📍 Canada