Opportunity
Clinical Research Coordinator (Carlsbad, CA)
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About the role
Clinical Research Coordinator I owning assigned studies from start-up through closeout in Southern California, Carlsbad, CA. On-site work includes participant visits, protocol procedures, clinical documentation and safety reporting. Bachelor’s degree with 1+ year of relevant experience, OR Associate’s degree with 3+ years, OR high school diploma with 4+ years of relevant experience and at least 1 year of CRC experience.
Key requirements
- • Bachelor’s degree with 1+ year of relevant experience, OR Associate’s degree with 3+ years, OR high school diploma with 4+ years of relevant experience and at least 1 year of CRC experience.
- • At least 1 year of relevant experience
- • Required skills: Clinical trial coordination, Independent participant visits and protocol procedures, Vital signs, EKGs, phlebotomy and laboratory processing, Source documents, CRFs and EDC documentation, Adverse event and protocol deviation reporting, Investigator, sponsor and CRO communication, Monitoring and audit readiness, Clinical trial management systems
Opportunity details
- • Workplace: On Site
- • Posted: Apr 28, 2026
- • Original advert language: English
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