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 workplace.

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 • Strong strategic thinking and communication skills

Embrace a leadership role in transforming GSK's clinical writing and drive impactful health solutions. #J-18808-Ljbffr

📌 Director Medical Writing at GSK (Winnipeg)
🏢 GSK
📍 Winnipeg