Clinical Research Coordinator (Oncology)
Core
Administratively coordinate clinical protocol implementation and logistical support for oncology clinical trials, ensuring data accuracy and regulatory compliance.
Role type
Clinical Research Coordinator (Oncology)
Builds
Clinical trial operations and patient data for hematology/oncology research studies
Domain
Healthcare / Clinical Research / Oncology
Deliverable
client delivery
Required skills
Protocol management, patient eligibility verification, data entry and maintenance, IRB liaison, recruitment strategy execution, consent process management, budget oversight, Good Clinical Practices (GCP) compliance
Preferred skills
None stated
Technologies
SKCCC Research Protocol Library, Clinical Research Management System, Oncology Information Systems
Responsibilities
Coordinate clinical study activities to ensure protocol adherence; Verify patient eligibility against protocol requirements; Manage patient registration and data entry in clinical databases; Conduct or oversee informed consent processes; Liaise with Institutional Review Board (IRB) and Principal Investigators; Assist in recruitment strategies and participant scheduling; Oversee study budget expenditures.
Seniority
Mid-level, hands-on operational role