Senior Clinical Research Coordinator - Cancer Center
Core
Recruit, screen, educate, and assist in the coordination of clinical research studies for patients at a Comprehensive Cancer Center.
Role type
Senior Clinical Research Coordinator
Builds
Clinical trial protocols, data documentation, and study budgets
Domain
Healthcare / Oncology / Clinical Research
Required skills
Patient recruitment, protocol compliance, data documentation, adverse event reporting, budget management, mentoring junior staff, regulatory knowledge (CFR, GCP, HIPAA), sample handling
Preferred skills
Master's degree, CCRC or CCRP certification
Technologies
Electronic health records, case report forms (CRFs), study management software
Responsibilities
Recruit and evaluate patient eligibility for clinical trials; maintain source documents and submit CRFs; mentor and train junior coordinators; report adverse events to PI, FDA, and sponsors; facilitate monitoring visits and audits; prepare contract documents and study budgets; collect and process biological samples; ensure supply inventory and track expenditures; review clinical data for GCP and FDA CFR compliance; assist with protocol feasibility and funding applications
Seniority
Senior, hands-on IC with leadership duties