Clinical Research Coordinator
Core
Coordinate and manage clinical trials, ensuring adherence to protocols and regulatory requirements while supporting patient recruitment, data collection, and documentation.
Role type
Clinical Research Coordinator I (hands-on IC)
Builds
Clinical trial data and patient records for medical research
Domain
Healthcare / Clinical Research
Deliverable
production ML models | product features | dashboards & analysis | client delivery | physical/clinical work
Required skills
Clinical study execution, informed consent, patient screening, vital signs monitoring, phlebotomy, sample processing, regulatory compliance (FDA/GCP/ICH), IRB coordination, data entry, patient retention
Preferred skills
English fluency, basic computer applications, organizational skills
Technologies
EDC systems, case report forms
Responsibilities
Conduct clinical studies according to regulations, perform defined study activities (screening, vital signs, ECGs), collect and record patient data, manage sample processing and shipping, ensure IRB approval and compliance, maintain patient files and source documents
Seniority
Junior, entry-level IC
