Clinical Research Coordinator III (RN)
Core
Coordinate care for patients on complex clinical research protocols (Phase 1-3 interventional trials) under medical supervision, ensuring regulatory compliance and data integrity.
Role type
Clinical Research Coordinator III (RN)
Builds
Clinical trial data, patient care records, and regulatory documentation for oncology/hematology studies.
Domain
Healthcare / Clinical Research / Oncology
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Protocol implementation, GCP/ICH/FDA guideline compliance, informed consent execution, adverse event reporting, study medication dispensing, data collection and verification, budget assessment, IRB/IEC document management, critical thinking, independent judgment.
Preferred skills
Oncology experience, EMR system experience, EDC system experience, CTMS experience.
Technologies
MS Office (Word, Excel, PowerPoint, Outlook), Electronic Medical Records (EMR), Clinical Trial Data Entry Systems (EDC), Clinical Trial Management Systems (CTMS)
Responsibilities
Assess subject eligibility against inclusion/exclusion criteria, conduct informed consent discussions, review and interpret diagnostic test results, report and follow up on adverse events, maintain inventory of investigational products, collect and verify accurate clinical data, manage monitoring visit preparations and follow-ups, develop study budgets.
Seniority
Mid-level, independent execution