
Real World Evidence Manager
Posted 16 hours ago

Posted 16 hours ago
This is a fully remote position, open to applicants in United States.
• Oversee the implementation of both retrospective and prospective Real-World Evidence (RWE) studies utilizing claims data, EMR/EHR data, and proprietary iRhythm clinical datasets.
• Operationalize study protocols, analytical plans, variable definitions, and statistical methodologies.
• Employ advanced epidemiological techniques such as propensity score matching, instrumental variables, difference-in-differences, interrupted time series, and survival analysis.
• Guarantee the reproducibility, auditability, and documentation of analytical pipelines.
• Develop and maintain budget impact models, cost-effectiveness models, and payer decision-support tools.
• Convert clinical evidence into economic inputs while accurately characterizing uncertainty.
• Create and update economic tools aimed at payers for client engagements.
• Execute sensitivity analyses, scenario modeling, and probabilistic analyses in accordance with HTA standards.
• Act as the main statistical programmer for RWE and health economic initiatives.
• Design and maintain the analytical data infrastructure, which includes datasets, codebooks, data dictionaries, and quality control processes.
• Collaborate with data vendors, CROs, and internal data science teams to access, cleanse, and validate data assets.
• Implement and sustain version-controlled analytical repositories.
• Prepare scientific abstracts, posters, and manuscripts for conferences and peer-reviewed journals.
• Translate complex analytical results for payer, clinical, and executive audiences.
• Co-author or contribute to health economic dossiers, coverage submissions, and payer value tools.
• Collaborate with Medical Affairs, Clinical Research, Commercial, and Payer Relations teams.
• Represent analytical workflows in stakeholder engagements.
• Mentor interns and junior analysts in research methodology, data analysis, and scientific writing.
• Master's or doctoral degree (MS, MPH, PhD) in Health Economics, Epidemiology, Biostatistics, Public Health, or a highly quantitative related field.
• A minimum of 3 years of progressive experience in Health Economics and Outcomes Research (HEOR), Real-World Evidence (RWE), or health economic analytics within the pharmaceutical, biotech, diagnostics, or digital health sectors (or a comparable academic/consulting background).
• Advanced proficiency in at least two of the following: R, Python, SAS, STATA for statistical analysis and data management.
• Proven experience in designing and executing observational studies using claims or EMR data.
• Strong history of developing health economic models (Budget Impact Models, Cost-Effectiveness Analysis, cost-utility models).
• Record of peer-reviewed publications or equivalent demonstrated scientific output (abstracts, posters, dossier contributions).
• Strong analytical judgment with the ability to conduct rigorous analyses and communicate methodological choices effectively.
• Preferred: PhD in Epidemiology, Biostatistics, Health Economics, or a related field.
• Preferred: Previous experience in cardiac electrophysiology, digital diagnostics, or ambulatory monitoring.
• Preferred: Understanding of US reimbursement structures (CMS, Medicare Advantage, commercial payers) and their evidentiary requirements.
• Preferred: Experience with NCQA/HEDIS measure development or quality measurement frameworks.
• Preferred: Familiarity with data platforms such as Optum Clinformatics, IBM MarketScan, TriNetX, or Komodo Health.
• Preferred: Experience with Tableau or similar visualization platforms.
• Competitive salary and performance-based bonuses.
• Comprehensive health, dental, and vision insurance.
• Retirement savings plans with company matching.
• Opportunities for professional development and continuous learning.
• Flexible working hours and remote work options.
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