HEOR Consultant

Contract Length: 12 months

Target Start Date: January 2027

Location: Fully remote (U.S.)

Schedule: Full-time, 40 hours per week

Position Overview

Our client is a leading medical device company with a rapidly advancing continuous glucose monitoring (CGM) product portfolio. The Health Economics and Outcomes Research (HEOR) team identifies, plans, and executes post-market real-world evidence (RWE) and health economics studies to demonstrate the clinical and economic value of its products and support global healthcare system access.

The team is seeking a hands-on HEOR Consultant to support a broad and evolving portfolio of research initiatives. This consultant will contribute to health economic modeling, real-world data analysis, health outcomes research, and scientific publications. Assignments may include analyzing medical claims data, developing or adapting cost-effectiveness models for international markets, supporting reimbursement and health technology assessment submissions, and contributing to multiple smaller projects as business needs evolve.

This is a project-based, flexible role requiring someone who can work independently, manage shifting priorities, and collaborate effectively with a cross-functional team.

Key Responsibilities

Health Economics and Modeling

• Conduct cost-effectiveness analyses using validated health economic models.
• Develop and modify budget impact models to evaluate the economic value of healthcare technologies.
• Apply health economic modeling methodologies, including Markov models and microsimulation, to support healthcare decision-making.
• Develop health economic value tools and dashboards using platforms such as BaseCase and Microsoft PowerPoint.
• Support economic evaluations for different international markets, potentially including country-specific modeling requirements.

Real-World Evidence and Outcomes Research

• Design real-world evidence study protocols and develop statistical analysis plans.
• Conduct statistical analyses of medical payer claims data, laboratory data, and other healthcare datasets.
• Work with real-world data sources, potentially including commercial claims databases such as Optum.
• Execute health outcomes research studies, including burden of illness, treatment patterns, healthcare resource utilization, and comparative effectiveness.
• Apply appropriate data management, statistical analysis, multivariate modeling, and other relevant analytical methods.
• Identify and interpret evidence gaps to support future research and product development initiatives.

Evidence Synthesis and Scientific Publications

• Analyze and synthesize clinical and economic literature to support research initiatives and evidence generation.
• Contribute to the preparation, review, and refinement of study reports, research protocols, statistical analysis plans, analytical documentation, and related study deliverables.
• Support the development of scientific manuscripts, conference abstracts, posters, and presentations.
• Contribute to international health technology assessment (HTA) and healthcare reimbursement submissions.
• Help communicate clinical and economic evidence to relevant healthcare stakeholders.

Cross-Functional Collaboration

• Collaborate with global launch teams, market development, clinical research, pricing, business development, and other internal stakeholders.
• Support communication of clinical and economic value propositions across different healthcare systems and markets.
• Manage multiple concurrent projects, adapting to changing priorities and timelines.
• Work independently while maintaining strong communication with the HEOR team and relevant project stakeholders.

Required Qualifications

• Master's degree minimum required and 5-10 years of industry experience.
• Hands-on experience in health economics, HEOR, outcomes research, epidemiology, or real-world evidence.
• Strong analytical skills, including data management, statistical analysis, and quantitative modeling.
• Experience using analytical software such as R, SAS, Stata, or comparable tools.
• Knowledge of health economic evaluation methodologies, including cost-effectiveness analysis and budget impact modeling.
• Understanding of clinical trial design, clinical and economic literature, and health economic analysis methods.
• Ability to interpret complex clinical and economic data and communicate findings clearly.
• Strong organizational skills, attention to detail, and ability to manage multiple projects and deadlines.
• Excellent written, verbal, presentation, and interpersonal communication skills.
• Ability to work independently, prioritize competing tasks, and follow assignments through to completion.
• Proficiency with Microsoft Office applications and common business software, including SharePoint and EndNote.
• Familiarity with diabetes management and the diabetes care industry.

Preferred Qualifications

• Experience working with continuous glucose monitoring (CGM) technologies, diabetes outcomes, or related medical device research.
• Experience analyzing medical claims data, including data from sources such as Optum.
• Demonstrated experience developing, adapting, or populating cost-effectiveness and budget impact models.
• Familiarity with Markov models, microsimulation, and health economic decision modeling.
• Experience supporting international HTA, reimbursement, or market access submissions.
• Track record of co-authoring scientific manuscripts, conference abstracts, posters, or other research publications.
• Experience with BaseCase or similar software for health economic value tools and dashboards.
• Experience collaborating with international teams and supporting research across multiple geographic markets.