The Clinical Research Coordinator II in Pediatric Oncology coordinates clinical research studies and ensures compliance with regulatory requirements while managing study operations. The role coordinates recruitment, screening, and enrollment of participants; obtains informed consent; manages study documentation; ensures compliance with study protocols and regulatory requirements; and collects, manages, and analyzes study data. The coordinator maintains study databases and regulatory documentation, tracks adverse events and protocol deviations, communicates with sponsors, IRBs, and research teams, and supports monitoring visits and audits. This job description is intended as a representative summary of the major responsibilities and accountabilities. Incumbents may be asked to perform other job-related tasks not specifically listed.
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Job Type
Full-time
Career Level
Mid Level