Harness your experience in regulatory content as a Senior Medical Writer within Amaris Consulting's hybrid work setting. Lead documentation efforts for global health authorities while shaping strategic regulatory submissions. As part of this agile team, you will take charge of developing and executing regulatory content strategies throughout the product lifecycle.

This includes managing clinical dossier preparations and ensuring compliance with global regulatory standards. By leading cross-functional collaborations, you will help resolve content-related challenges and maintain an organized workflow for submission documentation. Key Responsibilities:
Develop regulatory content strategies for global submissions




Oversee clinical dossier and safety documentation preparation
Review documents for clarity, consistency, and compliance
Collaborate with teams to ensure timely delivery
Mentor less experienced writers as needed Requirements:
Bachelor’s in a scientific discipline
At least 5 years in regulatory writing roles
Familiarity with ICH, GCP, GxP guidelines
Proven track record in managing regulatory projects
Proficiency in regulatory documentation tools Enhance your regulatory expertise and support vital submissions at Amaris Consulting.

📌 Senior Medical Writer Regulatory Content Specialist Mississauga
🏢 AMARIS GROUP
📍 Mississauga