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

Pf Health

Base: $176,600.00 - $294,300.00; bonus/equity: 20....
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Develop and execute pcoa strategies
Collaborate with cross-functional stakeholders
Align with regulatory and hta guidance
** Pfizer is seeking a Director for Health Technology Assessment (HTA), Value & Evidence (HV&E), focusing on Patient-Centered Outcomes Assessment (PCOA) strategies in clinical trials and observational studies. The role requires extensive experience in health outcomes research, particularly in clinical outcome assessment methodologies, and offers a hybrid work model with competitive salary and benefits. **

Job Summary

  • The Health Technology Assessment (HTA), Value & Evidence (HV&E) team is responsible for ensuring patients have affordable, timely access to medicines and vaccines by advancing innovative value and evidence solutions.
  • The PCOA Director is responsible for development and execution of fit-for-purpose PCOA strategies in clinical trials and observational studies to support registration, access, and reimbursement for Pfizer’s portfolio of innovative therapies.
  • The annual base salary for this position ranges from $176,600.00 to $294,300.00, with eligibility for a bonus target of 20.0% and long-term incentives.

Matching Summary

Match Score: 75

** Pfizer is seeking a Director for Health Technology Assessment (HTA), Value & Evidence (HV&E), focusing on Patient-Centered Outcomes Assessment (PCOA) strategies in clinical trials and observational studies. The role requires extensive experience in health outcomes research, particularly in clinical outcome assessment methodologies, and offers a hybrid work model with competitive salary and benefits. **

Salary

Base: $176,600.00 - $294,300.00; Bonus/Equity: 20.0% bonus target and long-term incentive program; Benefits: Comprehensive benefits including 401(k), paid time off, medical, dental, vision

Skills & Requirements

Must-have

  • Develop and execute PCOA strategies
  • Collaborate with cross-functional stakeholders
  • Align with regulatory and HTA guidance
  • Lead qualitative and quantitative evidence generation
  • Manage global network of consultants
  • Promote patient-centered outcome assessments

Nice-to-have

  • Foster collaborative knowledge sharing
  • Co-creation within team culture
  • Awareness of new research methods
  • Scientific rigor and initiative

Key Requirements

  • Advanced academic degree (MSc, MPH, PhD, DrPH, ScD, PharmD)
  • 5+ years experience with PhD/DrPH/ScD/PharmD or 7+ years with MSc/MPH
  • Advanced understanding of COA research methodology
  • Knowledge of regulatory guidance documents (FDA, EMA)
  • Experience with developing/validating COA measures
  • Experience preparing regulatory briefing documents
  • Technical competency in systematic literature reviews
  • Technical competency in ePRO/eCOA and linguistic validation
  • Strong project management skills

Work Rights

Permanent work authorization required

Tailored Resume

Cover Letter