Skip to content
Go to homepage

site

  • About
  • Benefits
  • Make a Difference
  • Search Jobs

This site uses cookies to improve the user experience! Would you like to allow cookies?

Cookie Settings

These cookies are necessary for the website to function and cannot be switched off in our systems. They are usually only set in response to actions made by you which amount to a request for services, such as setting your privacy preferences, logging in or filling in forms. You can set your browser to block or alert you about these cookies, but some parts of the site will not then work.

These cookies help us understand and improve the use and performance of our services including what links visitors clicked on the most, and how they interact with the various areas and features on our website and apps.

Clinical Research Coordinator

Torrance, CA
Apply Now Back to Search

Job Details

Job Location

Torrance Campus - Torrance, CA

Salary Range

$25.00 - $35.00 Hourly

Description

ABOUT US: The Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center is an independent, non-profit biomedical research organization located in Torrance, California. In dozens of laboratories throughout the campus, researchers are working to unravel the mysteries of heart and kidney disease, cardiac complications in newborns, chronic lung disease, skin cancer, sickle cell disease, disorders of the autoimmune system, and much more. Many of these projects are collaborative in nature, involving experts from different areas of specialization. Our discoveries have prevented blindness in newborns, enabled premature infants with fragile lungs to breathe and allowed children with rare, often fatal diseases to grow up healthy and strong.

Minimum Qualifications:

• Bachelor's degree or higher. • CITI • At least 6 years experience managing clinical trials • Previous experience as a Clinical Research Coordinator or similar role • Knowledge of clinical development processes and compliance management systems • Familiarity with clinical laboratory procedures and data collection methods • Strong attention to detail and ability to review documentation for accuracy • Excellent organizational skills and ability to manage multiple tasks simultaneously • Ability to work independently as well as part of a team

Responsibilities: • Management of trial master files • Coordinate clinical trials • Attend and productively participate in staff meetings and trainings as needed • Maintain high degree of responsibility for client confidentiality • Maintain a pleasant, courteous, tactful attitude with all contacts • Work with minimal supervision in exercising initiative in organizing and completing daily tasks

Apply Now Back to Search
Go to corporate home page
The Lundquist Institute Copyright © 2025
  • linkedin
  • twitter Twitter
  • facebook
Monster Strategic Talent Solutions