Clinical Research Coordinator
Core
Coordinate and manage oncology clinical trials, ensuring regulatory compliance and data integrity for cancer research studies.
Role type
Clinical Research Coordinator (IC)
Builds
Clinical trial operations and patient data for oncology research
Domain
Healthcare / Clinical Research / Oncology
Required skills
Clinical trial coordination, regulatory compliance (GCP/IRB), data entry and management, participant recruitment and consent, electronic data capture systems, medical terminology, study documentation
Preferred skills
Master's degree in clinical research or Public Health, CCRC certification, 5+ years clinical research experience
Technologies
Electronic data capture systems
Responsibilities
Manage day-to-day activities of clinical trials; coordinate participant recruitment, screening, and enrollment; collect and verify clinical trial data; prepare and submit regulatory documents to IRBs; inform and consent study participants; liaise with sponsors and external stakeholders; mentor junior research staff
Seniority
Mid-level, hands-on IC
