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Clinical Research Coordinator - Hematology/Oncology

UCLA Health
Flexible HybridRemotefull_timeVerifiedPosted 22 Jul 2026
💰 $122,000/yr($76,000/yr$122,000/yr)

About the role

General Information

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Work Location: Santa Monica, CA, USA
Onsite or Remote
Flexible Hybrid
Work Schedule
Monday-Friday, 8:00am-5:00pm
Posted Date
07/17/2026
Salary Range: $38.19 - 61.45 Hourly
Employment Type
2 - Staff: Career
Duration
Indefinite
Job #
31742

Primary Duties and Responsibilities

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The Department of Medicine is seeking a Data Coordinator to play a key role in advancing innovative clinical research that improves patient care and scientific discovery. In this dynamic position, you will oversee the day-to-day operational management of clinical research studies throughout the entire study lifecycle—from protocol development and study start-up through conduct and closeout. Working closely with Principal Investigators, sponsors, multidisciplinary clinical teams, and external partners, you will coordinate research activities, ensure regulatory compliance with institutional policies, FDA regulations, and ICH Good Clinical Practice (GCP) guidelines, and help drive the successful execution of one or more clinical trials. This is an excellent opportunity for a highly organized and collaborative professional to contribute to impactful research while supporting high-quality, compliant study operations and participant care.

Hourly range: $38.19-$61.45

Job Qualifications

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Required:

  • Bachelor's degree in related area and/or equivalent combination of education and experience.
  • Minimally 2+ years of previous study coordination or clinical research coordination experience
  • Interpersonal skills to effectively communicate information in a timely, professional manner and establish and maintain cooperative and effective working relationships with students, staff, faculty, external collaborators and administration and to work as a member of a team.
  • Ability to set priorities and complete ongoing tasks with competing deadlines, with frequent interruptions, to meet the programmatic and department needs, while complying with applicable University policies and federal and state regulations.
  • Analytical skills to assess clinical research protocols and regulatory requirements, define problems, formulate logical solutions, develop alternative solutions, make recommendations, and initiate corrective acti

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Company

UCLA Health

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