Job Description

Job Description

Job Description

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.

A top 10 pharmaceutical company with an immense amount of growth after releasing their at home COVID diagnostic tests is looking to bring on 200+ Quality Individuals through a massive hiring campaign. In their search for Quality Specialists, the organization is looking for individuals who will be responsible for reviewing and actioning customer complaints, as well as investigation into said complaints.
Job Responsibilities:
•\tConducting Post Market Activities and Post Market Surveillance
•\tManaging Customer and Product Complaint Investigation programs
Education and Experience:
•\t1 YR. of experience in a technical role in the medical device/pharma/biotech industry
•\tBachelor's degree
•\tComputer proficiency

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