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
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