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.
#J-18808-Ljbffr

📌 Medical Writing Asset Lead Director Role (Ontario)
🏢 GSK
📍 Ontario