Research Compliance Analyst, Pathology & Laboratory Medicine

About the position 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 Responsibilities • 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. Requirements • Minimum of 3 years of professional experience in clinical research. • In-depth knowledge of clinical research protocols, regulatory requirements, and human subject protection laws. • Experience working with local and external IRBs, scientific review committees, national cooperative group sponsors, industry sponsors, and federal and foundation funding organizations. • Must be able to report to work on-site (Westwood, Los Angeles) for a minimum of 3 days/week during first six months of hire. Nice-to-haves • Bachelor's degree preferred.Apply Now

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