Director, Hta, Value & Evidence (hv&e), Pcoa

pfizer.de

Unknown
Base: $176,600.00 to $294,300.00; bonus/equity: 20...
Hybrid
Patient-centered outcomes assessment (pcoa)
Clinical outcome assessment (coa) data expertise
Cross-functional collaboration
Pfizer is dedicated to delivering high value therapies and ensuring patients have affordable, timely access to medicines by advancing innovative value and evidence solutions

Job Summary

  • Pfizer is dedicated to delivering high value therapies and ensuring patients have affordable, timely access to medicines by advancing innovative value and evidence solutions.
  • The PCOA Director leads the development and execution of fit-for-purpose patient-centered outcomes assessment strategies in clinical trials and observational studies to support registration, access, and reimbursement.
  • This position offers a competitive salary range, bonus eligibility, comprehensive benefits, and requires hybrid work onsite 2 to 3 days per week.

Matching Summary

Pfizer is dedicated to delivering high value therapies and ensuring patients have affordable, timely access to medicines by advancing innovative value and evidence solutions.

Salary

Base: $176,600.00 to $294,300.00; Bonus/Equity: 20% bonus target plus share-based long term incentive; Benefits: Comprehensive health, retirement, and paid leave programs

Skills & Requirements

Must-have

  • Patient-centered outcomes assessment (PCOA)
  • Clinical outcome assessment (COA) data expertise
  • Cross-functional collaboration
  • Regulatory and HTA guidance alignment
  • Project management skills
  • Qualitative and quantitative research methods

Nice-to-have

  • Leadership and coaching abilities
  • Knowledge of psychometric analysis
  • Experience with ePRO/eCOA tools
  • Strong interpersonal and communication skills
  • Ability to work in matrix team environment

Key Requirements

  • Advanced academic degree in relevant health outcomes field
  • Minimum 5 years experience with PhD or 7 years with MSc in COA research
  • U.S. permanent work authorization required
  • Experience preparing regulatory briefing documents
  • Strong knowledge of FDA and EMA guidance

Work Rights

Permanent work authorization in the United States required

Tailored Resume

Cover Letter