Medical Writing Associate Director

Position: Medical Writing Associate Director Contract
Lead high-quality medical writing at Alexion as an Associate Director in Mississauga. Drive the clinical development portfolio through crafting essential regulatory documents over a 6-month contract.

In this role, you will be instrumental in authoring clinical protocols, reports, and regulatory submissions while ensuring compliance with internal and external standards. Your expertise in crafting impactful scientific narratives will help shape the clinical programs  position requires collaboration with various teams and mentoring less experienced writers to enhance document quality and efficiency.

Key Responsibilities:

• Author clinical study protocols and reports

• Manage high-quality medical writing deliverables

• Develop briefing packages for regulatory inquiries

• Ensure compliance with regulatory standards

• Mentor junior medical writing team members

Requirements:

• Experience in clinical regulatory medical writing

• Proficiency in MS Office suite for document creation

• Knowledge of global regulatory requirements

• Strong project management and organizational skills

• Excellent communication and presentation abilities

Elevate your career in medical writing by driving innovation and excellence in regulatory documentation at Alexion.
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