Clinical Trials Coordinator

1 week ago


San Diego, California, United States University of California Full time
Job Summary

We are seeking a highly motivated and detail-oriented Clinical Trials Coordinator to join our team at the University of California. The successful candidate will be responsible for coordinating multiple federally funded and industry-sponsored research studies involving human subjects.

Key Responsibilities
  • Interpreting research protocols and ensuring compliance with state and federal regulatory guidelines
  • Recruiting and screening subjects for eligibility, including obtaining vital signs, ECGs, height, and weight
  • Monitoring and reporting adverse events, toxicities, and protocol deviations
  • Scheduling subjects' visits and coordinating clinical, laboratory, and data activities
  • Processing and submitting laboratory specimens and collecting and entering research data
  • Maintaining accurate and complete clinical research files and patient medical charts
Requirements
  • Theoretical knowledge of biology, microbiology, social sciences, clinical sciences, and/or Bachelor's degree, and/or an equivalent combination of education and experience
  • Current CPR certificate or ability to attain within 2 months of hire date
  • Knowledge and experience of the clinical research setting, including protocols, principles, and standards
  • Ability to maintain subjects' confidentiality and communicate effectively with the research team
Preferred Qualifications
  • Certification as a clinical research associate or coordinator
  • Experience performing venipuncture and California Venipuncture license
  • Fluency in Spanish
Working Conditions

The successful candidate will be required to work at different clinical sites and may be required to travel. The position requires the ability to work independently with limited supervision and to communicate effectively with the research team.



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