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Senior Director, Global Program Leader - Oncology

Takeda
September 06, 2026
Full-time
Remote friendly (Boston, MA)
Worldwide
$333,190 - $333,190 USD yearly
Clinical Research and Development
Role: Senior Director, Global Program Leader - Oncology, Solid Tumors at Takeda, responsible for leading end-to-end global development and lifecycle management of oncology assets from discovery to market. Responsibilities: define asset strategy, oversee research, development, regulatory approval, launch, and commercialization activities; lead cross-functional global teams (including clinical, CMC, commercial, regulatory) and manage budgets; evaluate new opportunities and ensure alignment with patient access and company values. Requirements: MD, PhD, PharmD, or MBA; 10+ years industry experience with a focus on complex, global oncology projects, including NME approvals; strong leadership, strategic vision, stakeholder management, and matrix team management skills. Preferred: advanced science or business degree; experience with novel modalities like Cell or Gene Therapy; project management certification (e.g., PMI). High-Value: oncology (solid tumor), broad development stages, including late-phase trials, regulatory engagement, global launch, and lifecycle management; experience managing large-scale or rare disease programs; willingness to travel 20-25%, hybrid onsite in Boston. Collaboration: leads the Global Program Team (GPT) and liaises with internal stakeholders and external partners; reports to senior management. Work Setup: hybrid Boston, full-time, exempt.