Regulatory Compliance Officer - Jonsson Cancer Center

The UCLA Jonsson Comprehensive Cancer Center (JCCC)—one of only 56 NCI‑designated Comprehensive Cancer Centers nationwide—is recognized for excellence in cancer research, clinical care, education, and community impact. Its mission is to accelerate discoveries that prevent and cure cancer, drive innovation in care, train future scientific leaders, and partner with the community to improve health outcomes across Los Angeles and beyond.

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.