Global Development Lead, Internal Medicine (Sr. Director)

Role: Global Development Lead (GDL) oversees clinical development for Pfizer's Internal Medicine assets, serving as the clinical point of accountability within cross-functional teams. Responsibilities include designing and gaining endorsement for clinical development and regulatory strategies, leading study execution and interpretation, and contributing to regulatory submissions and product labeling. The GDL manages partnerships with internal teams and external stakeholders, providing therapeutic area expertise and leading innovative approaches in patient engagement and digital health. Qualifications: BS with 12+ years or PhD with 7+ years in clinical/industry settings, with experience in late-stage cardiometabolic development, including type 2 diabetes. Must possess deep knowledge of global regulatory standards, GxP, and clinical trial design, along with leadership experience managing large teams. High-value details: Focus on late-stage clinical trials with global regulatory and reimbursement considerations, including pediatric plans; up to 30% travel; hybrid work setup in the U.S. The role requires strong scientific credibility, strategic influence, and leadership in complex matrix environments.