Clinical Research Supervisor, Pathology & Laboratory Medicine

General Information

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Work Location: Los Angeles, USA Onsite or Remote Fully On-Site Work Schedule Monday – Friday, 8:00am – 5:00pm Posted Date 04/04/2025 Salary Range: $83800 - 179400 Annually Employment Type 2 - Staff: Career Duration Indefinite Job # 23180

Primary Duties and Responsibilities

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At UCLA Health, our world-renowned researchers are driven by a shared passion for discovery, working tirelessly to uncover life-saving breakthroughs, innovative therapies, and cutting-edge technologies. By joining our team, you'll apply your specialized knowledge and make a lasting impact on the lives of patients and their families.

As a Clinical Research Supervisor for the Department of Pathology & Laboratory Medicine, you will play a critical role in overseeing the day-to-day activities of our clinical research operations. You will lead and guide a dedicated team while ensuring that all clinical research operations run smoothly from initiation to close-out. 

Other primary duties include:

• Lead and mentor clinical research staff, providing guidance and support to ensure successful research contract execution.

• Assign and track tasks, ensuring efficient workload distribution and adherence to project timelines.

• Manage the full lifecycle of research projects, overseeing operations from initiation through close-out.

• Serve as the primary liaison between Principal Investigators (PIs), research sponsors, Institutional Review Boards (IRBs), and ancillary departments, ensuring seamless communication

• Lead activities around quality improvement, SOPs, formulating strategy, and processes.

Salary Range: $83,800.00 – $179,400.00/year

Job Qualifications

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• Minimum of 5 years of experience in a clinical research environment, with a strong understanding of clinical trial processes.

• Bachelor’s degree or equivalent professional experience in a related field.

• Clinical Research Certification (CCRP, ACRP, or similar) is preferred.

• Proven experience in clinical trials budgeting, with the ability to effectively manage the preparation, review, and oversight of clinical research budgets.

• Demonstrated success in leading teams (e.g. projects, committees, and/or cross-functional teams).

• Experience working with local and external IRBs, scientific review committees, national cooperative group sponsors, industry sponsors, and f