Regulatory Compliance Officer - Jonsson Cancer Center

This position supports regulatory compliance for complex clinical research studies and ensures adherence to federal, state, sponsor, and institutional requirements. The role manages regulatory submissions, maintains high-quality documentation, and collaborates with study monitors to ensure timely, compliant study activation and ongoing study oversight. Key Responsibilities: • Review clinical research protocols and prepare, manage, and submit all regulatory documents required by UCLA, FDA, NCI, IRB, and study sponsors. • Maintain complete and accurate regulatory files; ensure timely collection of essential study documents. • Work with study monitors to address queries and ensure compliance with all applicable laws, regulations, and policies. • Audit and monitor interventional clinical trials overseen by the JCCC Data and Safety Monitoring Board (DSMB). • Review external monitoring/audit reports for institutional oncology trials and track required follow-up actions. • Maintain and update the JCCC Clinical Trial Database to meet UCLA, FDA, and NCI reporting requirements. • Interpret regulations and determine applicability to JCCC studies; communicate compliance expectations to study teams. • Review and approve patient eligibility for DSMB-monitored studies according to established guidelines. Salary: $6,868.75 - $14,315 monthly