RN Oncology Clinical Research Coordinator
Core
Coordinates and manages the conduct of clinical trials within a health system, ensuring compliance with regulations and protocol requirements while managing investigational products and patient data.
Role type
Clinical Research Coordinator (Oncology)
Builds
Clinical trials for pharmaceutical/biotech sponsors
Domain
Healthcare / Clinical Research
Deliverable
client delivery
Required skills
Clinical trial coordination, regulatory compliance (ICH/GCP), patient recruitment and retention, adverse event reporting, data management (CTMS), informed consent processes, investigational product handling, source document verification, protocol adherence
Preferred skills
Registered Nurse (RN) licensure, Certified Clinical Research Coordinator (CCRC), IATA certification, CITI training
Technologies
CTMS, Electronic Health Record (EHR)
Responsibilities
Coordinate multiple clinical trials simultaneously; maintain accurate financial records and billing; ensure compliance with ICH/GCP guidelines and local/federal regulations; manage investigational product storage and dispensing; report Serious Adverse Events to PI, monitor, and sponsor; verify subject eligibility and prescreen via EHR; prepare and verify source documents and case report forms; educate patients and families on study protocols; support site audits and monitoring visits.
Seniority
Mid-level, hands-on IC