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Takeda Pharmaceutical Companyposted 2 months ago
$169,400 - $266,200/Yr
Full-time - Director
Remote - Boston, MA
1,001-5,000 employees
Chemical Manufacturing

About the position

The Director of Global Evidence & Outcomes at Takeda Pharmaceutical plays a crucial role in the development and commercialization of innovative therapies. This position is responsible for leading the development and execution of integrated evidence generation plans and research studies, ensuring that the evidentiary needs of patients, healthcare providers, regulators, and payers are met. The director collaborates with cross-functional teams to inform product strategies and provides leadership in real-world evidence and patient-centered value initiatives throughout the product lifecycle.

Responsibilities

  • Contribute to product strategy through membership on matrix teams and interactions with cross-functional partners.
  • Provide real-world evidence and patient-centered value leadership for Takeda products from early development through commercialization.
  • Lead the integrated evidence generation sub team and develop the integrated evidence generation plan.
  • Communicate findings from studies to internal and external audiences effectively.
  • Collaborate with product teams to inform program strategy and prepare for internal governance reviews.
  • Assess and identify value evidence requirements from stakeholders throughout the product lifecycle.
  • Ensure local evidence needs are met in line with product strategy.
  • Develop and execute GEO strategies to support evidence needs as defined in the integrated evidence generation plan.
  • Manage external research partners to ensure projects are scientifically rigorous and relevant.
  • Prepare and review clinical and outcomes research protocols and reports.

Requirements

  • Doctoral degree in a relevant discipline (e.g., health services research, epidemiology) plus 8+ years of practical experience, or a Master's degree plus 10+ years of practical experience.
  • Experience in performing epidemiology and outcomes research, including COAs, in various settings.
  • Demonstrated experience in conducting complex observational and/or COA studies.
  • Ability to communicate scientific evidence with strong written and verbal presentation skills.
  • Experience in drug development and launch is desirable.

Nice-to-haves

  • Oncology experience preferred.
  • Record of high-quality, peer-reviewed publications.
  • Ability to influence without authority, particularly at senior levels.

Benefits

  • Medical, dental, and vision insurance
  • 401(k) plan with company match
  • Short-term and long-term disability coverage
  • Basic life insurance
  • Tuition reimbursement program
  • Paid volunteer time off
  • Company holidays
  • Well-being benefits
  • Sick time and paid vacation accrual
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