Clinical Research Coordinator - Cancer Center
Core
Recruit, screen, and educate patients for clinical trials; manage data collection, documentation, and adverse event reporting for cancer research studies.
Role type
Clinical Research Coordinator (Cancer Center)
Builds
Clinical trial data and patient enrollment for NCI-designated cancer research
Domain
Healthcare / Oncology / Clinical Research
Required skills
Clinical trial regulations (CFR, GCP, HIPAA), Study budget management, MS Office, Phlebotomy assistance, Adverse event reporting, Protocol compliance, Quality assurance audits
Preferred skills
Certified Clinical Research Coordinator (CCRC), Certified Clinical Research Professional (CCRP), Bachelor's degree
Technologies
MS Office
Responsibilities
Recruit and evaluate patient eligibility for clinical trials; Maintain source documents and submit case report forms (CRFs); Recognize and report adverse events to PI, FDA, and sponsors; Perform study procedures per protocol; Assist with phlebotomy and sample collection; Track study expenditures and submit reimbursement requests; Participate in quality assurance audits and monitoring visits.
Seniority
Mid-level, hands-on IC