Lead medical writing strategy as the Director of Medical Writing Asset Lead at GSK. Shape clinical documents and accelerate product approvals in a hybrid work environment.

In this pivotal role, you will leverage your scientific, operational expertise, and leadership within a matrix organization. Your focus will be on crafting high-quality clinical documents for global regulatory submissions while driving process improvements. This position emphasizes collaboration, innovation, and the ability to influence with a focus on Hepatology assets and accelerated submissions.

Key Responsibilities:
• Develop clinical document strategy throughout drug life cycles
• Lead matrix teams and manage CROs to produce documents
• Deliver large submissions independently,



ensuring compliance
• Act as lead author on complex clinical documents
• Create training materials and mentor teams on medical writing

Requirements:
• PhD, PharmD, MPH, MSc, or equivalent degree
• Extensive clinical regulatory writing experience
• Proven project management and leadership skills
• Experience with accelerated submissions globally
• Robust strategic thinking and communication skills

Embrace a leadership role in transforming GSK's clinical writing and drive impactful health solutions.
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📌 Director Medical Writing at GSK (Ontario)
🏢 GSK
📍 Ontario