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Director, HTA, Value & Evidence, Obesity Early Pipeline
PfizerPfizer HEOR Director shaping evidence strategy for early-pipeline obesity medicines. Guiding clinical, economic, and real-world studies to improve global patient access.
Posted 8/13/2026full-timeNew York City • New York • 🇺🇸 United StatesLead💰 $176,600 - $294,300 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in Health Economics and Outcomes Research (HEOR) strategy, evidence generation, and patient access initiatives, with a strong focus on obesity and non-obesity products. Proficient in managing complex non-interventional studies and collaborating with cross-functional teams to drive strategic partnerships and research collaborations.
Highest-signal resume keywords
HEOR Strategy DevelopmentHealth Economic ModelingPatient-Reported OutcomesProject ManagementCross-Functional Team Leadership
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
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Hard Skills
Health EconomicsEpidemiologyHealth Services ResearchStatistical AnalysisReal-World Evidence StudiesObservational Study DesignEconomic ModelingTechnical Deliverable DisseminationClinical Trial DesignEvidence Generation
Soft Skills
Excellent Communication SkillsOrganizational SkillsDetail-OrientedProactive Problem SolvingAbility to Manage Multiple Projects
Certifications & Qualifications
Graduate Degree (MSc, MPH, PhD)
Industry Keywords
Clinical TrialsPatient AccessNegotiationsRegulatory GuidanceMarket Access StrategyStrategic PartnershipsHealthcare PolicymakersVendor ManagementMatrix OrganizationDrug Development Process
About the role
Key responsibilities & impact- Provide strategic input into clinical trial designs and analysis to support negotiations, reimbursement, and patient access
- Lead evidence generation strategy for Internal Medicine assets, focusing on obesity and non-obesity products
- Coordinate local country and regional input on evidence needs and incorporate it into global market access strategy
- Lead design and execution of global HEOR studies, including network meta-analyses, non-interventional studies, and economic models
- Develop patient-reported outcomes strategy and incorporate humanistic and economic endpoints into clinical trials
- Oversee evidence generation activities and dissemination of technical deliverables
- Partner with internal stakeholders to disseminate HEOR materials in accordance with regulatory guidance and internal SOPs
- Develop strategic partnerships and research collaborations with external experts, healthcare policymakers, payers, and academic and community settings
- Manage health economics and outcomes research supporting patient access to early-pipeline obesity and non-obesity products
- Collaborate with Primary Care GASP, US Market Access, cross-functional, and country teams
Requirements
What you’ll need- Graduate degree required, such as MSc, MPH, or PhD
- 7+ years of experience with MSc/MPH/MBA degree, or 5+ years with PharmD/PhD/DrPH in HEOR or related fields
- Expertise in HEOR strategy and evidence development
- Knowledge of health economics, epidemiology, health services research, or research-focused public health
- Expertise in health economic modeling, patient-reported outcomes, statistics, and real-world evidence studies
- Technical and methodological expertise in registries and observational study design, implementation, analysis, and interpretation
- Ability to independently manage complex non-interventional study projects
- Knowledge and understanding of the drug development process
- Excellent oral and written English communication skills
- Ability to assess project and program value and prioritize according to business priorities
- Strong project management abilities, including contracting, budgeting, and vendor management
- Ability to manage multiple complex projects with significant budgets, competing deadlines, and shifting priorities
- Experience leading cross-functional teams and guiding junior team members
- Skilled in functioning within a matrix organization
- Organized and detail-oriented, with ability to anticipate needs and work proactively
- Comfortable responding to unexpected demands with tight timelines
- Ability to travel domestically and internationally
- Ability to work in all US time zones
- Candidates must be authorized to be employed in the U.S. by any employer
- Permanent work authorization in the United States required; U.S. work visa sponsorship is not available
Benefits
Comp & perks- Participation in Pfizer’s Global Performance Plan with a bonus target of 20.0% of base salary
- Eligibility to participate in Pfizer’s share based long term incentive program
- 401(k) plan with Pfizer Matching Contributions
- Additional Pfizer Retirement Savings Contribution
- Paid vacation
- Paid holiday and personal days
- Paid caregiver/parental and medical leave
- Medical, prescription drug, dental and vision coverage
- Potential relocation assistance based on business needs and/or eligibility