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Truveta · 5 days ago

Senior Research Epidemiologist

Greater Seattle Area

Full-time

Hybrid

Senior Level

$142K/yr - $180K/yr

5+ years exp

Truveta is the world’s first health provider led data platform with a vision of Saving Lives with Data. They are seeking an experienced Senior Research Epidemiologist to lead and execute high-quality, client-driven epidemiological and health services research, focusing on real-world evidence studies for life sciences and healthcare decision-making.

AnalyticsData ManagementHealth Care

No H1B

Responsibilities

Lead and execute end-to-end epidemiological and real-world evidence studies, ensuring scientific rigor, transparency, and regulatory relevance

Design and oversee study protocols, statistical analysis plans (SAPs), study reports, and manuscripts, including post-authorization safety studies (PASS)

Support or lead studies focused on drug safety in special populations, including pregnant people and neonatal outcomes, where applicable

Ensure research outputs are suitable for regulatory submissions, responses, and post-marketing commitments

Uphold best practices in study conduct, reporting, and Good Pharmacoepidemiology Practices (GPP)

Apply advanced epidemiologic methods across study types such as:

Post-authorization safety studies (PASS)

Drug safety monitoring and pharmacovigilance

Comparative effectiveness research

Health Economics and Outcomes Research (HEOR)

Disease surveillance and signal detection

Collaborate closely with analytics and data science teams to review results, assess robustness, and interpret findings

Leverage or interpret outputs from surveillance and signal detection tools, including TreeScan, where applicable

Stay current with evolving regulatory guidance, observational research methods, and industry standards, including expectations for pregnancy safety evaluation

Serve as a primary research point of contact for customers, including life sciences partners and regulatory-focused stakeholders

Manage project timelines, resources, deliverables, and risks across multiple concurrent studies

Clearly communicate study design, methodology, and findings to internal teams, clients, and external stakeholders

Build and maintain trusted relationships with customers seeking regulatory-grade real-world evidence, including drug safety and pregnancy-focused research

Qualification

EpidemiologyPharmacoepidemiologyStatistical programmingObservational studiesHealth services researchElectronic health recordsProject managementCommunication skillsCollaborationProblem solving

Required

Master's or PhD in Epidemiology, Public Health, Biostatistics, Health Policy, or a related field

5+ years of experience in epidemiological, pharmacoepidemiology, or health services research, including leadership or project management responsibilities

Demonstrated experience designing and executing observational studies using real-world data

Strong hands-on experience with statistical programming (R and/or Python)

Experience working with electronic health records (EHRs), claims data, or other real-world healthcare data sources

Proven ability to manage complex, client-facing projects and deliver high-quality outputs under tight timelines

Excellent written and verbal communication skills, including presenting technical concepts to diverse audiences