Director, HTA, Value & Evidence (HV&E), Obesity Early Pipeline
$176,600–$294,300 year
On-siteNew York City, New York, United States
Job Summary
Provide strategic input into clinical trial designs and analysis to enable successful negotiations with global payer and regulatory decision makers. Lead the development of evidence generation strategies for Internal Medicine assets, focusing on obesity and non-obesity products, while coordinating input from local country/regional teams. Design and execute global health economics and outcomes research studies, including network meta-analyses and economic models, from concept through publication. Develop patient-reported outcomes strategies and incorporate humanistic and economic endpoints into clinical trials to build comprehensive evidence aligned with asset strategy. Partner with internal stakeholders to disseminate HEOR materials per regulatory guidance and establish strategic partnerships with external experts and payers. This role supports Pfizer's mission to ensure patients have affordable, timely access to innovative medicines by driving optimal patient access for early pipeline products.
Required Qualifications
- Graduate degree required (e.g. MSc, MPH, PhD)
- 7+ years of experience with MSc/MPH/MBA degree
- 5+ years with PharmD/PhD/DrPH in HEOR or relevant related fields (health economics, epidemiology, health services research, or other research-focused public health field)
- Expertise in HEOR strategy, evidence development, fundamental health services research methods and tools, including health economic modeling, patient-reported outcomes, statistics, and real-world evidence studies including technical and methodological aspects of registries and observational study design, implementation, analysis and interpretation
- Capable of independently managing complex non-interventional study projects
- Knowledge and understanding of drug development process
- Excellent interpersonal skills required: ability to understand and respond to multiple internal and external customers
- Excellent oral and written English communication skills
- Demonstrated ability to assess anticipated value for projects/programs to ensure alignment to business priorities and prioritize accordingly
- An “execution mindset” focused on getting things done quickly and simply
- Strong project management abilities (contracting, budgeting, vendor management) essential
- Demonstrated ability to manage multiple projects (multitask) involving complex processes, significant budget, competing deadlines and rapidly shifting priorities and expertise in stakeholder engagement
- Leadership in cross-functional teams (e.g. influence medical, clinical, and commercial teams constructively and without conflict); strategic thinking, and ability to guide junior team members
- Skilled in functioning within a matrix organization
- Organized and detail oriented with the ability to anticipate needs and to work proactively to prioritize & address/resolve
- Change oriented, comfortable responding to unexpected demands with tight timelines
- Ability to travel travel domestically and internationally
- Ability to work in all US time zones
- Location: US any Pfizer site or Europe any Pfizer site
- NOT eligible for Relocation Package
- This position is hybrid and requires working onsite 2 to 3 days per week
- Candidates must be authorized to be employed in the U.S. by any employer
- U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future
- This position requires permanent work authorization in the United States
Desired Qualifications
- Knowledge and experience in obesity / internal medicine space
- Experience with HTA organizations such as NICE, CADTH, PBAC, ICER and other HTA groups
- Previous experience with early-stage development, clinical trials, and patient-reported outcomes
- world study design and implementation
- Experience with developing early economic models to inform early clinical development and early pricing
- Experience in supporting global obesity / internal medicine launch
- Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity
- Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use
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