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 setting. 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.

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