Head of Evidence Generation, COA HTA and PED

Takeda Pharmaceutical Co.

Zürich

Remote

CHF 273,000 - 376,000

Full time

25 hours ago
Be an early applicant

A complete application in a minute

Tailored resume and cover letter, ready to send.

Get past ATS filters

Job summary

Takeda Pharmaceutical Co. seeks a Head of HTA, COA, and PED in Global Evidence Generation. You will lead a team delivering fit-for-purpose COA endpoints, PED strategies, and high-quality evidence to support HTA and payer differentiation worldwide.

Collaboration with internal and external stakeholders is essential to shape methods and guidelines for evolving global health authorities. The role emphasizes strategic decision-making, training raters, and advancing evidence generation to support

Qualifications

  • Fifteen or more years of experience in evidence generation, HTA, COA, PED, or related field.
  • Advanced degree in a scientific, clinical, epidemiologic, quantitative, or health outcomes discipline.

Responsibilities

  • Lead a team of experts for COA endpoint development, validation, execution, and quality control across regulatory, payer, physician, and patient needs.
  • Drive generation and communication of high-quality, fit-for-purpose evidence for HTA and payer evaluations globally.

Skills

15+ years exp
HTA knowledge
Team leadership
Global experience
Stakeholder engagement
Rater training knowledge
Policy environment understanding

Education

Advanced degree in science/health outcomes

Job description

Job Description

About the Role:

The Head of HTA, COA, and PED in Global Evidence Generation is responsible for leading a team of experts to develop, validate, and execute fit-for-purpose clinical outcome assessment (COA) endpoints, patient experience data (PED) strategies and high-quality evidence generation to support health technology assessment (HTA) and payer differentiation around the world.

This highly strategic role will drive early and innovative strategic decision making and high-quality execution for clinical outcome assessment, PRO (patient reported outcomes), and PED to support study execution, labeling, differentiation, payer and HTA interactions, and patient focus, in collaboration with internal and external stakeholders. They will engage actively with internal and external bodies to shape and interpret the rapidly changing requirements from global health authorities and build partnerships to shape methods and guidelines.

How You Will Contribute:

  • Lead a team of experts focused on clinical outcome assessment endpoint development, validation, execution, and quality control across regulatory, payer, physician, and patient needs
  • Drive the generation and communication of high-quality, fit-for-purpose evidence to support health technology assessment and other payer evaluations globally to demonstrate the value of Takeda’s assets
  • Lead early strategic review of clinical outcome assessment selection and implementation to support study execution, labeling, differentiation, payer and health technology assessment discussions, and patient focus
  • Train and monitor clinical outcome assessment raters to ensure quality, consistency, and compliance
  • Develop team expertise in health technology assessment methods in a rapidly changing environment, with a focus on Joint Clinical Assessment and the Inflation Reduction Act
  • Build capabilities in clinical outcome assessments and patient experience data, with an emphasis on using these tools to differentiate and demonstrate value
  • Accelerate evidence generation processes and strengthen alignment with local country teams to support scientifically robust, timely launches and health technology assessment submissions
  • Build and sustain external partnerships that help influence methods and guidelines for the evolving regulatory and access environment
  • Represent Takeda in external interactions with health authorities, payers, and external organizations focused on patient experience data, clinical outcome assessment, and health technology assessment
  • Ensure strong compliance with evolving requirements from global regulatory agencies and health authorities
  • Drive operational excellence through clear governance, prioritization, resource allocation, and performance metrics.
  • Coach, develop, and retain a high-performing team; support succession planning and capability building across the function.

Preferred Qualifications:

  • Fifteen or more years of experience in evidence generation, health technology assessment, clinical outcome assessment, patient experience data, or a closely related field
  • Advanced degree in a scientific, clinical, epidemiologic, quantitative, or health outcomes discipline required.
  • Deep knowledge of study design, healthcare data analysis, clinical outcome assessment, health system landscaping, and the regulations and guidelines related to health technology assessment, clinical outcome assessment, and patient experience data
  • Proven experience leading teams of experts and building capability in a complex and rapidly evolving global environment
  • Strong track record of working with health authorities, payers, and external organizations
  • Experience with evidence generation strategies that support global access, regulatory, and value communication needs
  • Ability to build cross-functional alignment and support timely evidence generation for launches and submissions
  • Understanding of clinical outcome assessment rater training, monitoring, and quality processes and guidelines
  • Advanced knowledge of health technology assessment methods, with experience in a rapidly changing policy environment
Locations
Zurich, Switzerland

Base Salary Range:

CHF273,100.00 - CHF375,540.00

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.

Worker Type
Employee
Worker Sub-Type
Regular
Time Type
Full time
Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Head of Global Access Scientific Communications
Head of Global Access Scientific Communications

Takeda Pharmaceutical Co. • Zürich

On-site
CHF 223,000 - 307,000
Head of Global Access Scientific Communications
Head of Global Access Scientific Communications

Takeda Pharmaceutical Co. • Glattbrugg

On-site
CHF 223,000 - 307,000
Global Head of Evidence Generation & HTA Strategy
Global Head of Evidence Generation & HTA Strategy

Takeda Pharmaceutical Co. • Zürich

Remote
CHF 273,000 - 376,000
Senior EU Regulatory Lead GI&I / Director
Senior EU Regulatory Lead GI&I / Director

Takeda Pharmaceutical Co. • Zürich

On-site
CHF 177,000 - 244,000
IBU Medical Lead Nephrology & LCM
IBU Medical Lead Nephrology & LCM

CHE - 8036 Takeda Pharmaceuticals International AG • Glattbrugg

On-site
CHF 189,000 - 260,000
IBU Medical Lead, GI
IBU Medical Lead, GI

CHE - 8036 Takeda Pharmaceuticals International AG • Glattbrugg

On-site
CHF 189,000 - 260,000
Director, Modality Excellence - Indirect Processes, Quality, Engineering & Maintenance and Warehouse
Director, Modality Excellence - Indirect Processes, Quality, Engineering & Maintenance and Warehouse

Takeda Pharmaceutical Co. • Zürich

On-site
CHF 177,000 - 244,000
Global Pricing Lead (24-Month Fixed-Term Contract)
Global Pricing Lead (24-Month Fixed-Term Contract)

Takeda • Zürich

On-site
CHF 169,000 - 233,000
Global Medical Core Capability Strategy Lead
Global Medical Core Capability Strategy Lead

8036 Takeda Pharmaceuticals International AG • Switzerland

On-site
CHF 189,000 - 260,000
Director, Modality Excellence - Indirect Processes, Quality, Engineering & Maintenance and Warehouse
Director, Modality Excellence - Indirect Processes, Quality, Engineering & Maintenance and Warehouse

Takeda • Zürich

On-site
CHF 177,000 - 244,000