Research Registered Nurse
Core
Coordinate care for patients on clinical research protocols, manage investigational products, and ensure data integrity for oncology trials.
Role type
Clinical Research Coordinator III (RN)
Builds
Phase 1-3 interventional clinical trials
Domain
Oncology / Clinical Research
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Protocol implementation, GCP/ICH/FDA compliance, Informed consent execution, Adverse event reporting, Study medication dispensing, Data collection and verification, Budget development, IRB/IEC documentation
Preferred skills
Oncology experience, EMR systems, EDC systems, CTMS
Technologies
MS Office, EMR, EDC, CTMS
Responsibilities
Assess subject eligibility against inclusion/exclusion criteria, Conduct informed consent discussions, Dispense study medication, Report adverse events, Collect and verify clinical data, Manage study budgets and billing
Seniority
Mid-level, independent IC