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Clinical Data Specialist

Cambridge HQ💼 Full-time🗓 2026-07-14 → 2026-07-31

Core

Conduct detailed EHR reviews to identify potential clinical trial candidates, support patient recruitment, maintain research databases, and ensure accurate documentation in the patient pre-screening process.

Role type

Clinical Data Specialist

Builds

Patient recruitment pipelines and research databases for clinical trials in GI, hepatology, obesity, and cardiology

Domain

Healthcare technology / Clinical research

Deliverable

production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work

Required skills

EHR data review, study protocol interpretation, database management, regulatory compliance documentation, data entry, scheduling coordination

Preferred skills

Clinical research operations experience, GCP guidelines knowledge, Salesforce/CTMS platform familiarity, biotech/startup environment experience

Technologies

Electronic Health Records (EHRs), Clinical Trial Management Systems (CTMS), Customer Relationship Management (CRM), Microsoft Office Suite, Google Workspace, Adobe Acrobat, Salesforce

Responsibilities

Review electronic health records to identify patients qualifying for active clinical research studies; Interpret study protocols and eligibility criteria to determine appropriate patient populations; Build and maintain databases of potential study participants; Document patient pre-screening activities and findings; Collaborate with research sites to support participant recruitment; Perform accurate data entry into clinical research databases

Seniority

Individual Contributor

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