AD HEOR
Listed on 2026-08-28
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Healthcare
Clinical Research, Medical Science
EPM is partnering with an innovative commercial-stage biotechnology company seeking an Associate Director of HEOR & Real-World Evidence to join a growing global evidence generation team.
This individual will play a key role in shaping evidence strategies that support market access, reimbursement, and value demonstration for a recently launched specialty therapy addressing a significant unmet medical need. The position offers high visibility across Medical Affairs, Clinical Development, Biostatistics, Market Access, and Commercial functions.
We're looking to speak with candidates who bring:
- Significant HEOR, RWE, or Epidemiology experience within pharma or life sciences consulting
- Expertise designing and executing observational studies and real-world evidence programs
- Experience with claims, EHR, and other real-world data sources
- Publication and scientific dissemination experience
- A track record partnering cross-functionally to support access and value initiatives
- Develop and execute global RWE strategies and evidence-generation plans to support reimbursement, access, and value demonstration.
- Design and manage retrospective, prospective, pragmatic, and implementation science studies using real-world data sources.
- Analyze claims, EHR, and other real-world datasets to demonstrate treatment effectiveness, burden of disease, and healthcare outcomes.
- Lead dissemination activities including publications, congress presentations, and technical deliverables.
- Provide strategic evidence support for payer, HTA, and market access needs globally.
This is an excellent opportunity to join a well-funded organization during a period of substantial growth and contribute to evidence generation strategy for a first-in-class therapy.
Desired Skills and ExperienceStrong expertise in observational research, real-world database analyses, and advanced statistical methodologies.
Experience generating evidence to support commercialization, reimbursement, and patient access objectives.
Liver disease, metabolic disease, NASH/MASH, or specialty pharmaceutical experience is advantageous.
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