Associate Director, Global HEOR and Evidence Generation

New
E
Encoded Therapeutics Inc.Biotechnology, gene therapy
Workable locations: United StatesFull-TimeDirector
Salary not disclosed
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Job Details

Experience
Minimum of 5 years of relevant pharmaceutical industry or specialized consulting experience.

Requirements

  • Hold a master's degree (MS, MPH), MD, PharmD, or PhD in HEOR, Epidemiology, Biostatistics, Public Health, Psychology, or a related quantitative or scientific discipline.
  • Have at least 5 years of relevant pharmaceutical industry or specialized consulting experience.
  • Demonstrate expertise in at least two core HEOR disciplines, such as epidemiology, economic modeling, observational research, or mixed-methods research.
  • Have experience designing and executing observational research, Patient Experience Data (PED), and Clinical Outcome Assessments (COA/PRO).
  • Have experience with psychometric validation and health economic modeling.
  • Demonstrate ability to lead HEOR research from conceptualization and protocol development through peer-reviewed publication and defense before global health authorities.
  • Have direct experience preparing HEOR components for global regulatory dossiers and Health Technology Assessment submissions.
  • Have project management experience across complex projects, budgets, and external vendor partnerships in global matrix environments.
  • Have working knowledge of pharmaceutical compliance frameworks, legal and regulatory review processes, and clinical trial designs.
  • Be willing to travel domestically and internationally as needed.
  • Preferred: PhD in HEOR or a related scientific discipline.
  • Preferred: Experience in rare genetic disorders, neurology, or advanced therapeutics such as gene and cell therapies.
  • Preferred: Experience supporting late-stage development, pre-launch commercialization, and global launch execution.

Responsibilities

  • Shape and support execution of global HEOR strategies for product approval, clinical differentiation, and patient access.
  • Align evidence generation with global HTA requirements and the US payer and value assessment landscape.
  • Execute HEOR-related commercial strategies for asset launches.
  • Partner with Clinical, Regulatory, Commercial, Medical Affairs, and Patient Advocacy on global evidence-generation strategy.
  • Lead HEOR research initiatives, including literature reviews, natural history, disease burden, observational research, COA/PRO, and health economic and epidemiological modeling.
  • Lead evidence landscape assessments and data gap analyses to inform asset strategy and identify data sources.
  • Oversee research planning, budgets, execution, dissemination, external vendors, and scientific partnerships.
  • Maintain scientific rigor across proposals, protocols, and statistical analysis plans and defend research in internal and external forums.
  • Develop HEOR best practices, governance frameworks, and educational resources across the organization.
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