Global Development Lead, Internal Medicine (Sr. Director)

Role: Global Development Lead (GDL) overseeing clinical development for Pfizer's Internal Medicine assets, focusing on global regulatory approval and reimbursement. Responsibilities: lead cross-functional clinical teams, develop and endorse clinical development plans and protocols, support regulatory submissions including safety reports and product labels, and engage external stakeholders for strategic insights. Accountable for trial design, feasibility, and operational execution, including pediatric studies and innovative strategies such as digital patient engagement. Requirements: BS with 12+ years or PhD with 7+ years in clinical/industry research, with experience in cardiometabolic late-stage development, particularly type 2 diabetes. Extensive knowledge of global clinical development, regulatory standards, and GxP compliance. Preferred: experience managing large, cross-functional teams, and a strong track record in clinical drug development within the biopharma sector. High-Value: expertise in late-stage clinical trials, regulatory submissions, cardiometabolic therapeutic areas, and pediatric planning. Collaboration: works with trial clinicians, external stakeholders, and internal teams. Work setup: hybrid model, with up to 30% travel; location within commuting distance to Pfizer facilities.