Elevate your career at Alexion as a Lead Medical Writer responsible for high-quality clinical documents. This 6-month contract emphasizes regulatory submissions and scientific clarity within a adaptable work setting.

As an Associate Director of Medical Writing, you will drive medical writing efforts across diverse clinical programs. Your expertise will be crucial in authoring protocols, study reports, and regulatory submissions. By translating complex data into clear narratives, you contribute to groundbreaking medicines that change lives.

Key Responsibilities:



• Author clinical documents including protocols and reports • Develop briefing packages for health authority inquiries • Support clinical teams by delivering high-quality documents • Negotiate timelines across functions • Mentor junior medical writers and ensure adherence to standards

Requirements: • Experience in clinical regulatory writing and submissions • Proficiency in writing investigational documents • Strong knowledge of global regulatory and ICH standards • Excellent project management and negotiation skills • Advanced proficiency in MS Office suite

Your skills in medical writing and regulatory understanding will significantly impact patient solutions at Alexion.

📌 Lead Medical Writer at Alexion (Mississauga)
🏢 Alexion Pharmaceuticals,Inc.
📍 Mississauga