Senior Global Patient Access Strategy Lead (Hybrid)

Takeda; Cambridge (MA); Hybrid; USD 137,000 - 215,000; Full time

Job summary

Takeda seeks a leader to develop and advance Global Patient Access strategies across programs, ensuring alignment with enterprise priorities, regulatory requirements, and product lifecycles. Based in Cambridge, MA, this hybrid role collaborates with global teams to deliver data-driven, scalable programs.

The role requires advanced degrees with years of experience in clinical research or expanded access within pharma or CRO, and prefers individuals with experience managing such programs and a

Qualifications

• PhD or PharmD with 3+ years of relevant experience in clinical research or expanded access.
• Master's degree with 6+ years; or Bachelor's degree with 8+ years of relevant experience.
• Advanced degree in a health science field is preferred.
• Experience managing expanded access programs is preferred.

Responsibilities

• Develop and advance Global Patient Access strategies across programs.
• Align strategies with enterprise priorities, regulatory requirements, and product lifecycle needs.
• Support data-driven, technology-enabled strategies and global execution.
• Use digital platforms to support program execution, tracking, and visibility.
• Partner with systems teams to use data and analytics to improve design and reporting.
• Promote data quality and compliant data handling across programs.
• Represent Global Patient Access on cross-functional teams and influence strategy and execution.
• Coordinate with Medical, Clinical, Regulatory, Supply, and Commercial teams.

Education

PhD/PharmD with 3+ years experience

Master's degree with 6+ years

Bachelor's degree with 8+ years

Job description

Takeda seeks a leader to develop and advance Global Patient Access strategies across programs, ensuring alignment with enterprise priorities, regulatory requirements, and product lifecycles. Based in Cambridge, MA, this hybrid role collaborates with global teams to deliver data-driven, scalable programs.

The role requires advanced degrees with years of experience in clinical research or expanded access within pharma or CRO, and prefers individuals with experience managing such programs and a