Director GHEOR

EPM Scientific is partnered with a rapidly growing, Commercial-Stage Biopharmaceutical company to hire a Director of GHEOR. Our client is seeking a health economics & outcomes research expert to drive evidence generation strategy and align with Global Medical Affairs and business objectives to optimize patient access, pricing, and reimbursement across US and international markets.

• Integrate input from U.S., European, and other global teams into a comprehensive evidence plan supporting market access and lifecycle management.
• Design and execute HEOR studies, including network meta-analyses and real-world evidence projects, from concept through publication.
• Develop HTA and launch deliverables such as value dossiers, systematic literature reviews, economic models, and innovative tools for payer engagement and reimbursement.
• Provide strategic input into clinical trial design to inform payer and regulatory decisions.
• Ensure compliant dissemination of HEOR materials per regulatory guidance and internal SOPs.
• Build strategic partnerships with external experts, policymakers, payers, and academic institutions to support asset strategies and evidence generation.
• Manage GHEOR budget planning, forecasting, and resource allocation for U.S. and international initiatives.
• Oversee external vendor contracts and timelines to ensure deliverables are on time, within scope, and within budget.
• Mentor and train team members, fostering continuous development and aligning publication activities with strategic objectives.
• Ensure all activities adhere to company SOPs, industry standards, and regulatory requirements.
• Uphold the highest ethical standards in all external engagements.
• Willingness to travel up to 30%, primarily U.S. with occasional international travel; ability to work across time zones as needed.

Requirements:

• Graduate degree in health economics, epidemiology, health services research, or a related field
• 12-15+ years of HEOR/ RWE/ Outcomes Research experience
• Deep knowledge of international regulatory and value assessment bodies (e.g., ICER) and HTA agencies (e.g., NICE, CADTH)
• Expertise in economic modeling, patient-reported outcomes (PROs), statistics, and real-world evidence studies. Must have experience executing complex observational studies.
• Deep knowledge of drug development process and payer landscape in the United States
• Strong interpersonal and influencing abilities to collaborate effectively with internal and external stakeholders across cross-functional, matrixed teams.
• Highly organized with expertise in project management, including budgeting, contracting, vendor oversight, and managing multiple priorities under pressure.
• Outstanding written and verbal communication skills, with experience creating technical and value-focused materials for diverse audiences.
• History demonstrating a proactive approach to problem-solving and adaptability in dynamic/ fast-paced environments.

Please Note: This position does not offer visa sponsorship. Candidates must be authorized to work in the United States without the need for current or future sponsorship.

**Applicants who do not meet the above requirements will not be considered for this role.