Global Development Lead, Internal Medicine (MD, Sr. Director)

Role: Global Development Lead (GDL) responsible for clinical development of Pfizer's Internal Medicine assets. Objectives include leading cross-functional teams, designing clinical strategies, and supporting global regulatory submissions. Responsibilities encompass creating and endorsing Clinical Development Plans, overseeing trial design and feasibility, providing therapeutic expertise, and contributing to regulatory documents like PBRERs and labels. The GDL also engages external stakeholders, supports regulatory submissions, and ensures compliance with GxP standards. Qualifications: MD or DO with 8+ years in clinical research, preferably with endocrinology or cardiometabolic expertise, and experience in late-stage development (Phases 2-3) in biopharma. Proven leadership, cross-functional influence, and knowledge of ICH/GCP are essential. High-value biopharma specifics include focus on type 2 diabetes and metabolic disorders, with responsibilities spanning clinical trials, regulatory submissions, and strategic planning. The role involves up to 30% travel, is hybrid (onsite ~2.5 days/week), and may include international regulatory activities. Candidate must demonstrate scientific credibility, leadership, and agility in a complex, matrixed environment.