Join GSK as the Medical Writing Asset Lead Director to enhance regulatory submissions. Guide clinical document strategy and unleash innovation in a hybrid work setup. As a Director at GSK, you will utilize your vast experience in medical writing and submissions, particularly in Hepatology areas.

This role enables you to lead significant activities that impact product approvals and ensures alignment across teams. You will be responsible for managing both internal and external resources to maintain high standards in clinical document creation and submission processes. Key Responsibilities:
Contribute to clinical document lifecycle management
Oversee planning and production with matrix teams
Propose solutions for effective large submissions
Act as lead author for regulatory document content
Mentor teams on regulatory writing and practices Requirements:
Advanced degree (PhD, PharmD, etc.) required
Significant experience in regulatory submissions
Track record in project management and leadership
Familiarity with global submission requirements
Excellent communication and influencing skills Lead GSK's medical writing initiatives and advance your career in impactful healthcare solutions.

📌 Medical Writing Asset Lead Director Role Mississauga
🏢 GSK
📍 Mississauga