The Clinical Research Coordinator Pediatric Oncology coordinates clinical research studies and ensures compliance with regulatory requirements while managing study operations. The role supports recruitment, screening, and enrollment; informed consent and study documentation; protocol compliance; data collection, management, and analysis; study databases and regulatory records; adverse-event and protocol-deviation tracking; communication with sponsors, IRBs, and research teams; and monitoring visits and audits. This job description is intended as a representative summary of the major responsibilities and accountabilities. Incumbents may also be requested to perform other job-related tasks.
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Job Type
Full-time
Career Level
Mid Level