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 managementOversee planning and production with matrix teamsPropose solutions for productive large submissionsAct as lead author for regulatory document contentMentor teams on regulatory writing and practicesRequirements:Advanced degree (PhD, PharmD, etc.) requiredSignificant experience in regulatory submissionsTrack record in project management and leadershipFamiliarity with global submission requirementsExcellent communication and influencing skillsLead GSK's medical writing initiatives and advance your career in impactful healthcare solutions.#J-18808-Ljbffr

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