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Director, Global Evidence & Outcomes

Takeda
Full-time
Remote friendly (Boston, MA)
United States
$174,500 - $274,230 USD yearly
Medical Affairs

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Role Summary

Director, Global Evidence & Outcomes

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 and consultative expertise for Takeda product(s) from early development through launch and commercialization.
  • Lead the integrated evidence generation sub team for products under development and develop the integrated evidence generation plan.
  • Lead the development, execution, and communication of real-world evidence and COA strategies to support regulatory submissions, product labelling, access and commercialization.
  • Communicate findings from these studies to relevant internal and external audiences.
  • May manage a small team depending on size of global programs/disease areas.

Qualifications

  • Combination of academic training and practical experience in outcomes research (oncology experience preferred) with a Doctoral degree plus 8+ years of experience or a Masters plus 10+ years of experience.
  • Practical experience in performing epidemiology and outcomes research and/or COAs.
  • Regulator and/or HTA/payer policy-makers experience.
  • Drug development experience and launch experience desirable.
  • Demonstrated experience in complex observational and/or COA studies and ability to communicate findings to internal and external audiences.
  • Ability to work collaboratively in a multicultural, cross-functional team environment.
  • Strong written and verbal communication skills; ability to lead cross-functional teams.
  • Networking, communication, and influencing skills; ability to manage multiple complex research studies.
  • Ability to influence without authority, especially with senior-level individuals.

Skills

  • Evidence generation planning
  • Real-world evidence and COA methodology
  • Clinical development plans and regulatory strategy alignment
  • Project management and external partner management
  • Scientific communication and publication planning
  • Stakeholder engagement with regulators, HTAs/payers

Education

  • Doctoral degree in a relevant discipline (e.g., health services research, epidemiology, public health, statistics) or a Masters with extensive experience.

Additional Requirements

  • Travel: approximately 25% - 50% domestic and international