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

Role: Global Development Lead (GDL) in Pfizer's Internal Medicine R&D, accountable for clinical development strategy and execution of assigned assets, including trial design, regulatory submissions, and cross-functional leadership. Responsibilities: lead clinical development teams, oversee protocol design, contribute to regulatory documents (e.g., IND, BLA), develop global clinical plans, and engage external stakeholders. Act as a therapeutic area expert, providing input on target profiles, safety review, and data interpretation. Lead efforts for regulatory submission support, risk-benefit evaluation, and product labeling. Requirements: MD or DO, 8+ years in clinical research within biopharma, preferably cardiology and cardiovascular outcomes trials, with extensive knowledge of global regulations, ICH/GCP standards, and drug development processes. Preferred: experience managing large teams, designing complex trials, and working on late-stage assets. High-Value: Internal Medicine focus, cardiovascular endpoints, global regulatory environment, late-phase clinical development, and cross-disciplinary collaboration. Work setup: hybrid (onsite ~2.5 days/week) in the U.S., up to 30% travel; relocation support available.