Irvine Clinical Research

Irvine Clinical Research

Experienced Clinical Research Coordinator - Westside Los Angeles

Inglewood, CA · Principal

Sponsorship not specified$62k-$83kDetected 240 days ago
GCPClinical TrialsClinical ResearchFDA RegulatoryResearchCommunicationGxP

About the role

  • Our largest area of research is in Alzheimer's Disease prevention and treatment drug trials, and our doctors were the largest contributors in the world to the most recently FDA-approved medication in Alzheimer's Disease.
  • This role is ideal for a seasoned CRC (internally leveled as a CRC II, III, or IV depending on experience) who is ready to take ownership of complex Phase II and III clinical trials.
  • You will work closely with our Principal Investigators and clinical team to ensure the highest standards of data integrity, patient safety, and operational excellence.

Responsibilities

  • Timely and accurately enter, organize, and maintain study data across various electronic platforms (eSource, EDC, CTMS), proactively resolving queries.
  • Maintain impeccable regulatory and source documentation, ensuring the site is consistently prepared for sponsor monitoring visits and audits.

Nice to have

  • 2 to 4+ years of hands-on experience coordinating industry-sponsored clinical trials (prior experience in CNS, Neurology, or Psychiatry is a strong plus).

Skills

  • Demonstrated ability to navigate complex clinical trial management systems (CRIO eSource & CTMS) and EDC platforms quickly and accurately.
  • Equal Opportunity & Fair Chance Employer Irvine Clinical Research and its affiliates are Equal Opportunity Employers.

Compensation

  • $62k-$83k

Company info

  • Inglewood Clinical is part of the Irvine Clinical Research site network, the largest of its kind on the West Coast.
  • With 5 research centers in California, we are leaders in the search for new treatments in neurology, psychiatry, and obesity medicine.
  • We are seeking a dedicated and experienced Clinical Research Coordinator to drive trial success at our Oakland location.

Visa & Work Authorization

  • udit Readiness: Maintain impeccable regulatory and source documentation, ensuring the site is consistently prepared for sponsor monitoring visits and audits

This listing is sourced directly from Irvine Clinical Research's careers page and normalized into a canonical job model.