HEOR Consultant

HEOR Consultant III (Research Health Economist)

12-month Contract

Requirements

• Contribute to health economics projects by performing evidence synthesis, outcome research, and related analytical tasks under the direction of project leads.
• Support the generation of value evidence across the product life cycle in alignment with global payer and health technology assessment (HTA) requirements.
• Assist in developing protocols and the end-to-end execution of outcome research to support launch, commercialization, and payer-focused evidence generation.
• Conduct primary, secondary, and exploratory analyses based on approved protocols, including:
• HCRU cost modeling using difference-in-differences and GLM-based methods
• Dosage interval analyses
• Time-to-event analyses, including Kaplan–Meier
• Decision-analytic modeling, including Markov and simulation models
• Perform systematic literature reviews and meta-analyses to inform protocol development.
• Prepare and deliver proposals, technical reports, slide presentations, conference abstracts, manuscripts, and other deliverables with guidance from project leads.
• Communicate progress, issues, and findings to team members to support timely completion of project milestones.
• Present research findings internally and at professional scientific or industry conferences as assigned.
• Conduct targeted literature searches to identify key evidence and data inputs.
• Work independently on assigned tasks and collaborate effectively within cross-functional teams.
• Apply knowledge of clinical development, research study designs, and interpretation of clinical and real-world evidence.
• Apply qualitative and quantitative research methodologies.
• Apply knowledge of the pharmaceutical industry, global regulatory expectations, and product development processes across all life cycle stages.
• Apply knowledge of international healthcare systems and evolving HTA requirements.
• Work with open claims, closed claims, and electronic medical record (EMR) datasets.

Qualifications

• PhD in industrial engineering, operations research, mathematics, economics/health economics, pharmaceutical outcomes & policy, statistics, biostatistics, decision sciences, health services research, or a related field, with at least 3 years of experience in the pharmaceutical industry, contract research, or a related environment, including academia; OR
• Master’s degree in one of the above fields with at least 5 years of relevant experience in the pharmaceutical industry, contract research, or a related environment, including academia.
• Minimum 3+ years of experience in healthcare resource utilization (HCRU) analysis, HCRU cost modeling, difference-in-differences and GLM-based methods, dosage interval analyses, time-to-event analyses, and decision-analytic modeling, including Markov and simulation models.
• Proficiency in Microsoft Excel, SQL (Snowflake), R or Python, and SAS.
• 5+ years of experience in Excel, Python/R, and SQL.
• Highly motivated, detail-oriented self-starter who can follow directions, manage multiple priorities, and resolve complex issues in collaboration with team leads.
• Excellent interpersonal, written, and oral communication skills, with the ability to translate complex concepts into clear, actionable insights.