clinical research nurse II
Core
Conduct clinical trials involving patients or healthy volunteers, ensuring subject safety and data capture per study protocol.
Role type
clinical research nurse (IC)
Builds
clinical trial data and patient safety outcomes for pharmaceutical and biotech clients
Domain
clinical research / pharmaceutical trials
Deliverable
physical/clinical work
Required skills
clinical trial execution, patient care, informed consent, vital signs monitoring, ECG administration, regulatory compliance (FDA/GCP/ICH), data recording, IRB requirement management, patient recruitment and retention
Preferred skills
independent work, complex information analysis, decision-making, negotiation, influencing, organizational skills, computer proficiency, teamwork
Technologies
case report forms, EDC systems
Responsibilities
Conduct clinical studies per FDA/GCP/ICH guidelines; perform study activities including screening, vital signs, ECGs, and pregnancy tests; schedule subject visits; record patient data and test results; maintain source documents and patient files; report non-compliance; obtain and maintain IRB approval; interact with research site teams; manage patient communication and retention.
Seniority
Mid-level, hands-on IC
