Research Compliance Analyst, Pathology & Laboratory Medicine

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.

Salary Range: $76,200.00 - $158,800.00/year

* 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.

* Bachelor's degree preferred.

* 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.