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

Role: Global Development Lead (GDL) for Clinical Development within Pfizer's Internal Medicine R&D. Objective: Lead clinical development strategies and cross-functional teams for assigned assets, ensuring regulatory approval and global reimbursement. Responsibilities: oversee clinical trial design, execution, and interpretation; develop and endorse Clinical Development Plans and protocols; lead regulatory submissions, including INDs, IBs, and safety reports; provide therapeutic expertise in cardiometabolic conditions like type 2 diabetes; engage external stakeholders; ensure compliance with regulatory standards; and support product labeling and safety updates. Qualifications: MD or DO with 8+ years in clinical research, preferably with endocrinology or internal medicine focus; extensive knowledge of GxP, ICH/GCP, and global regulatory requirements; strong leadership, project management, and cross-functional collaboration skills; demonstrated success in late-stage development and regulatory submissions. High-Value: Focus on cardiometabolic diseases, late-stage development, global regulatory strategy, and cross-functional leadership in a hybrid work environment with up to 30% travel. Collaboration: Partner with internal teams (clinical, safety, statistics, commercial) and external stakeholders (regulatory bodies, advisory boards). Work setup: Hybrid, based in the U.S., with relocation support.