Evidence Generation TA Lead, GI2

USA - 3316 Takeda Development Center Americas, Inc.

Cambridge (MA)

On-site

USD 192,000 - 302,000

Full time

4 days ago
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Benefits offered by this job

Competitive base salary
Boston, MA location

Job summary

Takeda is seeking a Director-level leader to shape and guide evidence generation strategies for assigned assets across the product lifecycle. You will integrate stakeholder insights, emerging data, and changing evidence landscapes to inform decisions from registration to lifecycle management.

You will lead cross-functional teams across Medical, R&D, Market Access, and Evidence Generation to align priorities and ensure compliant, impactful evidence generation.

Qualifications

  • Doctorate or Master’s with extensive experience in medical affairs, clinical development, epidemiology, or related field.
  • Bachelor’s degree with substantial relevant scientific/quantitative background.
  • Experience supporting evidence strategy development and execution for products/assets/indications.
  • Knowledge of evidence generation across the product lifecycle and its role in stakeholder decisions.
  • Strong leadership and ability to manage multiple priorities in a matrixed environment.
  • Excellent communication and collaboration across functions and stakeholders.

Responsibilities

  • Lead evidence generation strategy for assigned assets across the product lifecycle.
  • Develop integrated evidence plans translating priorities into sequenced studies and dissemination activities.
  • Provide scientific oversight from concept to execution of studies.
  • Drive alignment across teams, governance forums, and external partners to enable timely evidence delivery.
  • Partner with functions and regions to support registration, launch, market access, and differentiation.
  • Engage external stakeholders and communicate evidence through advisory activities and scientific forums.

Skills

Evidence strategy
Project leadership
Cross-functional collaboration
Scientific communication

Education

PhD in medical/science
Master's degree in related field

Job description

About the Role

In this Director level role, you will help shape and lead evidence generation strategies for assigned assets or indications across the product lifecycle. You will play a key role in identifying evidence needs by integrating stakeholder insights, emerging data, evolving healthcare requirements, and changing evidence landscapes. Your work will contribute to informed decision-making, product registration, launch readiness, market access, differentiation, and lifecycle management. You will be part of a cross-functional environment that brings together colleagues across Medical, Research and Development, Market Access, Commercial, and Evidence Generation teams, as well as external experts. By developing and advancing integrated evidence strategies, you will help ensure that evidence priorities are aligned with business objectives and strategic plans while supporting scientifically rigorous, compliant, and impactful evidence generation activities.

How You Will Contribute
  • Lead evidence generation strategy for assigned assets or indications by identifying, prioritizing, and shaping evidence needs across the product lifecycle.
  • Develop and evolve integrated evidence plans that translate evidence priorities into sequenced evidence-generation and dissemination activities from early development through post-launch.
  • Guide evidence generation teams by setting strategic direction, driving stakeholder alignment, and supporting evidence-based decisions across complex environments.
  • Partner across functions and regions to identify evidence activities that support patients, business decisions, registration, launch, market access, and product differentiation.
  • Provide scientific oversight for evidence generation studies from concept through execution, interpretation, and communication to ensure quality, compliance, and impact.
  • Drive alignment and decision making across teams, governance forums, and external partners to enable timely and efficient evidence delivery.
  • Contribute to strategic planning and governance by integrating evidence priorities into key plans, submissions, recommendations, and lifecycle decisions.
  • Engage external stakeholders and communicate evidence through scientific exchange, advisory activities, scientific forums, and other external settings as appropriate.
Qualifications
  • Doctorate degree with 8+ years of experience, or master’s degree with 10+ years of experience, in medical affairs, clinical development, epidemiology, evidence generation, outcomes research, or a related field.
  • Bachelor’s degree with substantial relevant experience in a scientific, medical, or quantitative discipline.
  • Experience supporting evidence strategy development and execution for products, assets, or indications.
  • Working knowledge of evidence generation across the product lifecycle and its role in supporting stakeholder decisions across geographies.
  • Knowledge of study design, including randomized, observational, real-world evidence, and other fit-for-purpose evidence generation methods.
  • Strong project leadership skills with the ability to manage multiple priorities in a matrixed environment.
  • Strong communication and organizational skills with the ability to collaborate effectively across functions and stakeholders.
Compensation and Benefits

For Location: Boston, MA U.S.
Base Salary Range: $192,400.00 - $302,390.00
The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job. The actual base salary offered will be in accordance with state or local minimum wage requirements for the job location.

EEO Statement

Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.

Locations

Boston, MA

Worker Type

Employee Worker Sub-Type Regular Time Type Full time Job Exempt Yes

Legal Information

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Company Overview

Takeda is an industry-leading, global pharmaceutical company with an unwavering dedication to putting patients at the center of everything we do. We live our values of Takeda-ism – Integrity, Fairness, Honesty, and Perseverance – and are united by our mission to strive towards Better Health and a Brighter Future for people worldwide through leading innovation in medicine. Here, everyone matters and you will be a vital contributor to our inspiring, bold mission. At Takeda, you will make an impact on people’s lives – including your own.

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