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Director, Global Value and Health Economics, Outcomes Research
Jazz Pharmaceuticals. Lead global and US payer evidence strategy across marketed assets in Jazz’s neurology portfolio .
Posted 10/31/2026full-timeRemote • Pennsylvania • United StatesLead💰 $212,000 - $318,000 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) with a focus on post-marketing strategies, economic modeling, and evidence generation for biopharmaceutical products. Proven ability to collaborate with cross-functional teams and influence stakeholders while ensuring compliance with regulatory standards.
Highest-signal resume keywords
Health Economics ExpertisePost-Marketing HEOR StrategyEconomic Modeling ProficiencyCross-Functional CollaborationRegulatory Compliance Knowledge
ATS Keywords
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Hard Skills
Economic ModelingComparative Effectiveness StudiesReal-World Evidence GenerationBudget Impact ModelingStatistical AnalysisData ValidationHealth Technology Assessment (HTA)PharmacoeconomicsEpidemiological MethodsPost-Authorization Studies
Soft Skills
Exceptional Communication SkillsInfluencing SkillsMentorship AbilitiesTeam LeadershipPresentation Skills
Tools & Technologies
Healthcare DatabasesInteractive Economic ModelsStatistical SoftwareBudget ModelsValue Dossiers
Industry Keywords
Biopharmaceutical IndustryManaged Care LandscapeRare DiseaseMarket AccessPayer EngagementHealth PolicyICERFDA GuidanceAMCP DossiersNeurology Portfolio
About the role
Key responsibilities & impact- Lead global and US payer evidence strategy across marketed assets in Jazz’s neurology portfolio
- Maximize brand potential, defend value, secure expanded access, and drive post-launch evidence generation
- Develop evidence strategies for label expansions, new formulations, line extensions, and expanded patient subpopulations
- Partner with Medical Affairs, Clinical Development, and Biostatistics on Phase 3b/4, pragmatic, and expanded access studies
- Lead rare disease registries, natural history extensions, and post-authorization safety/efficacy studies
- Design comparative effectiveness, adherence, burden-of-illness, and real-world data studies
- Co-create HTA reassessment strategies and analytical packages with EU/INT HEOR teams
- Direct updates to Global Value Dossiers, systematic literature reviews, and meta-analyses
- Lead AMCP dossiers, unbranded value summaries, and state Medicaid submission dossiers
- Design and train teams on interactive economic models and reactive scientific presentations
- Ensure US HEOR materials comply with FDAMA Section 114, the 21st Century Cures Act, and FDA HCEI guidance
- Evaluate outcomes-based risk-sharing agreements and real-world endpoint tracking frameworks
- Monitor US health policy, ICER, and value framework developments
- Formulate and execute cost-effectiveness, cost-utility, budget impact, and cost-offset modeling strategies
- Build and adapt economic models using mature clinical and real-world data
- Serve as GVHEOR representative in IEGP governance and align evidence initiatives with brand objectives
- Partner with Market Access and cross-functional teams on post-launch evidence initiatives
- Lead publications, manuscripts, and conference presentations
- Manage budgets, external HEOR consultancies, academic partners, and CROs
- Provide mentorship and technical guidance to evidence and value generation staff
Requirements
What you’ll need- Master’s degree (MSc, MS, MPH) or PhD in Health Economics, Outcomes Research, Pharmacoeconomics, or a closely related quantitative field
- Minimum of 7–10 years of experience in HEOR, Global Value, or Health Economics within the biopharmaceutical industry or a top-tier HEOR consulting firm
- Extensive experience designing and executing post-marketing HEOR strategies, real-world comparative effectiveness studies, and evidence roadmaps supporting label expansions, line extensions, and value defense
- Comprehensive knowledge of the US managed care landscape and global HTA environments
- Proven technical expertise building, adapting, and validating economic models, including Markov, partitioned survival, microsimulation, and dynamic budget impact models
- Proven track record collaborating with US Market Access, Pricing/Contracting, and Payer Field Teams to develop compliant customer-facing tools, interactive budget models, and AMCP dossiers
- Demonstrated understanding of rare disease post-launch evidence challenges
- Working knowledge of major US and global healthcare databases and advanced epidemiological methods
- Demonstrated ability to work with regional HEOR teams, especially EU/INT
- Ability to balance evidence strategy with hands-on execution of complex technical deliverables
- Exceptional verbal, written, and presentation skills; ability to influence cross-functional teams and defend methodologies
- Experience with neurology assets preferred
- Track record leading HEOR strategy and evidence deliverables for marketed pharmaceutical products
- Launch lead for at least 2 assets as US HEOR lead, or country-level HTA lead
- Experience conducting post-marketing RWE, patient registry studies, and economic evaluations
- Strong peer-reviewed publication record in health economics and outcomes research
Benefits
Comp & perks- Discretionary annual cash bonus or incentive compensation
- Discretionary equity grants
- Medical insurance
- Dental insurance
- Vision insurance
- 401k retirement savings plan
- Flexible paid vacation