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Natera

Associate Director – Real-World Evidence, Observational Research

Natera

Associate Director of Real-World Evidence driving evidence initiatives for early cancer detection at Natera. Leading cross-functional research strategies and partnerships to inform product adoption and clinical use.

Posted 4/30/2026full-timeRemote • 🇺🇸 United StatesSenior💰 $146,400 - $183,000 per yearWebsite

About the role

Key responsibilities & impact
  • Lead the design and execution of real-world evidence studies, including retrospective database analyses and prospective observational studies.
  • Contribute to clinical evidence strategy for a defined product area, identifying where RWE can address key evidence gaps.
  • Translate clinical, scientific, and business questions into robust, decision-oriented study designs.
  • Proactively identify risks to study execution and implement mitigation strategies.
  • Lead to protocol development, including objectives/endpoints, eligibility criteria, data collection approaches, and analysis plans.
  • Partner with biostatistics and data science to ensure high-quality data analysis, interpretation, and reporting.
  • Drive medical data review, interpretation, and synthesis of findings.
  • Deliver clear, actionable insights that inform product strategy, clinical positioning, and market access.
  • Evaluate real-world product performance and identify opportunities to improve adoption, utilization, and outcomes.
  • Partner with Product and Medical Affairs to ensure real-world insights are fed back into product development.
  • Contribute to evidence planning by identifying where RWE can most effectively address key gaps.
  • Support prioritization of studies based on business impact, feasibility, and timing.
  • Ensure alignment between RWE, clinical studies, and broader evidence generation efforts.
  • Support development of publications, abstracts, and presentations to communicate evidence externally.
  • Partner with Medical Affairs and Market Access to translate evidence into compelling narratives for clinicians, KOLs, and payers.

Requirements

What you’ll need
  • Advanced degree (PhD, MPH, MS, PharmD, or equivalent) in epidemiology, health outcomes research, biostatistics, or related field.
  • 7–10+ years of experience in real-world evidence, observational research, or HEOR, ideally in industry.
  • Demonstrated experience leading the design and execution of observational studies across the full lifecycle (protocol through analysis and dissemination).
  • Strong understanding of real-world data sources (claims, EHR, registries) and their application to clinical and business questions.

Benefits

Comp & perks
  • Comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents.
  • Free testing for employees and their immediate families.
  • Fertility care benefits.
  • Pregnancy and baby bonding leave.
  • 401k benefits.
  • Commuter benefits.
  • Employee referral program.

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools
real-world evidenceobservational studiesprotocol developmentdata analysisdata interpretationrisk mitigation strategiesevidence planningclinical evidence strategybiostatisticshealth outcomes research
Soft Skills
leadershipcommunicationcollaborationproblem-solvingstrategic thinkinginsight deliveryprioritizationadaptabilitystakeholder engagementnarrative development
Certifications
PhDMPHMSPharmD