Senior Clinical Study Analyst - Cohort & Data Expert
TriNetX
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Job summary
TriNetX is seeking a Sr. Clinical Study Analyst in Cambridge, MA (hybrid) or US remote.
The role involves translating eligibility criteria into patient cohorts, applying standard coding schemes, and leading live demonstrations of TriNetX LIVE for pharma, CRO, and healthcare clients. You will collaborate with clinical feasibility and analytics teams, manage multiple engagements, mentor junior staff, and contribute to publications and knowledge sharing while ensuring data quality and
Qualifications
- Bachelor's degree or equivalent in health-related field.
- 5+ years in healthcare, clinical research, or pharma/CRO setting.
- Experience with patient data including EMR/claims.
- Familiarity with clinical data coding systems.
- Strong written, verbal, and presentation skills.
Responsibilities
- Translate eligibility criteria and query cohorts using TriNetX LIVE.
- Apply ICD, CPT, SNOMED coding to define cohorts.
- Understand clinical trial eligibility criteria and map to data sources.
- Lead live demos and trainings of TriNetX LIVE for users.
- Serve as primary contact for pharma, biotech, CRO, and healthcare clients.
- Handle high volume questions about platform capabilities.
- Collaborate with Clinical Feasibility & Analytics and Client Delivery teams.
- Mentor junior analysts and document feedback for product/usability.
Skills
Education
Tools
Job description
TriNetX is seeking a Sr. Clinical Study Analyst in Cambridge, MA (hybrid) or US remote.
The role involves translating eligibility criteria into patient cohorts, applying standard coding schemes, and leading live demonstrations of TriNetX LIVE for pharma, CRO, and healthcare clients. You will collaborate with clinical feasibility and analytics teams, manage multiple engagements, mentor junior staff, and contribute to publications and knowledge sharing while ensuring data quality and
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