Research Coordinator
Core
Supports clinical trial conduct by ensuring protocol compliance, managing patient screening and consent, and maintaining data integrity for oncology studies.
Role type
Clinical Research Coordinator (Oncology)
Builds
Clinical trial data and patient care records for oncology drug development
Domain
Healthcare / Clinical Research / Oncology
Required skills
Protocol compliance, patient screening, informed consent management, data abstraction, regulatory adherence, adverse event reporting, patient education, interdisciplinary collaboration
Preferred skills
Oncology clinical trial experience, Registered Nursing license, Research Coordination experience
Technologies
Electronic Data Capture (EDC), Clinical Research Forms (CRFs)
Responsibilities
Screen patients for study eligibility, obtain and maintain informed consent, coordinate study visits and procedures, document patient encounters and data in CRFs, report adverse events, ensure protocol adherence, educate patients and staff
Seniority
Mid-level, hands-on IC