Senior Research Epidemiologist

Senior Research Epidemiologist Truveta is the world’s first health provider led data platform with a vision of Saving Lives with Data. Our mission is to enable researchers to find cures faster, empower every clinician to be an expert, and help families make the most informed decisions about their care. Achieving Truveta’ s ambitious vision requires an incredible team of talented and inspired people with a special combination of health, software and big data experience who share our company values . Truveta was born in the Pacific Northwest, but we have employees who live across the country. Our team enjoys the flexibility of a hybrid model and working from anywhere. In person attendance is required at least once per year for an onsite meeting. For overall team productivity, we optimize meeting hours in the pacific time zone. We avoid scheduling recurring meetings that start after 3pm PT, however, ad hoc meetings occur between 8am-6pm Pacific time. #LI-remote Who We Need Truveta is rapidly building a talented and diverse team to tackle complex health and technical challenges. Beyond core capabilities, we are seeking problem solvers, passionate and collaborative teammates, and those willing to roll up their sleeves while making a difference. If you are interested in the opportunity to pursue purposeful work, join a mission-driven team, and build a rewarding career while having fun, Truveta may be the perfect fit for you. This Opportunity We are seeking an experienced Senior Research Epidemiologist to lead and execute high-quality, client-driven epidemiological and health services research. This role i s responsible for the end-to-end delivery of real-world evidence studies supporting life sciences, healthcare, and regulatory decision-making. The ideal candidate brings strong pharmacoepidemiology and /or regulatory-facing research experience . This is a highly collaborative, client-facing role that combines methodological leadership, project execution, and scientific communication. Key Responsibilities Research Leadership Execution 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. Apply advanced epidemiologic methods across various study designs. Collaborate closely with analytics and data science teams to review results, assess robustness, and interpret findings. Stay current with evolving regulatory guidance, observational research methods, and industry standards. Project Management 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. Qualifications Experience Required Qualifications Master’s or PhD in Epid emiology, Public Health, Biostatistics, Health Policy, or a related field. 7+ 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. 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. Highly Desired / Preferred Experience Hands-on experience with statistical programming (R and/or Python). Track record of peer-reviewed publications. ... (truncated, view full listing at source)