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Research Compliance Analyst, Pathology & Laboratory Medicine
Research Compliance Analyst, Pathology & Laboratory MedicineUniversity of California - Los Angeles Health • Los Angeles, CA, United States
Research Compliance Analyst, Pathology & Laboratory Medicine

Research Compliance Analyst, Pathology & Laboratory Medicine

University of California - Los Angeles Health • Los Angeles, CA, United States
1 day ago
Job type
  • Full-time
Job description

Description

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

Qualifications

  • 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.
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