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 - Robust 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 (Canada)
🏢 GSK
📍 Canada