Clinical Research Nurse
Core
Conduct clinical trials involving patients or healthy volunteers, ensuring subject safety and data capture per study protocol.
Role type
Clinical Research Nurse II (IC)
Builds
Clinical trial data and patient records for pharmaceutical and biotech clients
Domain
Clinical research / Life sciences
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
GCP/ICH regulations knowledge, patient safety monitoring, vital signs measurement, informed consent procedures, EDC data entry, IRB compliance, study recruitment and retention, source document management
Preferred skills
Independent work, complex information analysis, decision-making, negotiation, English fluency
Technologies
EDC systems, case report forms
Responsibilities
Conduct clinical studies per FDA/GCP guidelines, schedule subject visits, perform screening and protocol procedures (vital signs, ECGs), record patient data, manage IP accountability logs, report non-compliance, obtain/maintain IRB approval, promote company to ensure participant retention, attend site initiation meetings, handle patient bookings and follow-ups, maintain source documents and patient files
Seniority
Mid-level, hands-on IC