A passion for discovery inspires and motivates UCLA Health’s world-renowned researchers to diligently uncover incredible life-saving breakthroughs, innovative therapies, and next-generation technologies. Join us and make the most of your specialized knowledge and your passion for making a positive impact on the lives of others.

As the Research Compliance Analyst for the department of Pathology & Laboratory Medicine, you will provide compliance oversight for all clinical research studies. Primary duties include:

• Serve as the primary regulatory expert, assisting with writing and reviewing research protocols to ensure adherence to federal, state, and institutional regulations, policies, and sponsor requirements. 

• Oversee the regulatory coordination of clinical research contracts and studies.

• Review and submit research contract & study approvals, protocol amendments, and regulatory filings. 

• Develop and maintain regulatory documents such as IRB submissions, informed consent forms, and monitoring plans. 

• Liaise with regulatory agencies, sponsors, and institutional committees to ensure compliance. 

• Review complex research protocols, providing guidance on research applications, and ensuring compliance with laws and policies governing human subjects research and conflicts of interest. 

Note: This is a flexible hybrid position. The incumbent will be expected to work approximately 3 days per week on-site. Additional on-site days may be required depending on workflow and operational priorities.

Salary Range: $78,500.00 - $163,600.00/year