***Please note: This position is onsite and not remote. Candidates must be based in the Orange, CA area, as relocation assistance is not provided. Only individuals authorized to work in the U.S. will be considered.***
Job Title: Senior Clinical Research Coordinator (Liver Trials)
Job Type: Full-Time | On-Site
Job Location: Orange, CA
Job Salary: $90,000-$100,000 per year (based on experience)
Industry: Clinical Research | Hepatology | Phase IâIV Trials
About Us:
Join a fast-paced, compliance-driven research clinic specializing in liver disease trialsâfrom NASH and cirrhosis to hepatocellular carcinoma. The clinic partners with leading sponsors and CROs to deliver high-quality, audit-ready data and compassionate patient care.
Position Overview:
This is an on-site position in Orange, CA, and applicants must reside within a commutable distance of 50 miles or less or be able to independently relocate. THIS IS NOT A REMOTE POSITION.
Weâre seeking a Senior Clinical Research Coordinator (CRC) with hands-on experience in liver-focused clinical trials. Youâll lead study execution, regulatory coordination, and patient engagement across multiple protocols.
MUST HAVE - Experience in CRC in Liver/GI/Obesity studies
MUST HAVE - Regulatory experience
MUST HAVE - Fluency in Spanish
Key Responsibilities
⢠ââââCoordinate Phase IâIV liver trials, including screening, enrollment, and follow-up
⢠ââââManage regulatory submissions (IRB, CPHS), source documentation, and AE reporting
⢠ââââOversee biospecimen handling and lab coordination
⢠ââââMaintain CTMS and EDC systems (REDCap, Medidata, etc.)
⢠ââââMentor junior CRCs and support cross-functional study teams
Requirements
Qualifications
⢠ââââ3â5+ years of CRC experience in liver/hepatology trials
⢠ââââStrong knowledge of FDA, ICH-GCP, and HIPAA regulations
⢠ââââProficiency in CTMS, EDC platforms, and protocol adherence
⢠ââââExcellent communication and documentation skills
⢠ââââBilingual (Spanish/English) preferred
⢠ââââFamiliarity with California specific regulations
Certifications
⢠ââââGCP Training (Required)
⢠ââââHIPAA & Human Subjects Protection (Required)
⢠ââââCPHS Compliance Training (Required)
⢠ââââCCRC (Certified Clinical Research Coordinator) (Preferred)
⢠ââââCCRP (Certified Clinical Research Professional) (Preferred)
Salary :
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