Senior Clinical Research Coordinator (CRC)
Smarter HR Solutions LLC•Orange, CA
•$90,000 - $100,000•Onsite
About The Position
Join a fast-paced, compliance-driven research clinic specializing in liver disease trials—from 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. We’re seeking a Senior Clinical Research Coordinator (CRC) with hands-on experience in liver-focused clinical trials. You’ll lead study execution, regulatory coordination, and patient engagement across multiple protocols.
Requirements
- 3–5+ years of CRC experience in liver/hepatology trials
- Strong knowledge of FDA, ICH-GCP, and HIPAA regulations
- Proficiency in CTMS, EDC platforms, and protocol adherence
- Excellent communication and documentation skills
- Familiarity with California specific regulations
- GCP Training (Required)
- HIPAA & Human Subjects Protection (Required)
- CPHS Compliance Training (Required)
Nice To Haves
- CCRC (Certified Clinical Research Coordinator)
- CCRP (Certified Clinical Research Professional)
- Bilingual (Spanish/English) preferred
Responsibilities
- Coordinate Phase I–IV liver trials, including screening, enrollment, and follow-up
- Manage regulatory submissions (IRB, CPHS), source documentation, and AE reporting
- Oversee biospecimen handling and lab coordination
- Maintain CTMS and EDC systems (REDCap, Medidata, etc.)
- Mentor junior CRCs and support cross-functional study teams
Benefits
- Competitive salary + performance bonuses
- Health, dental, and vision coverage
- Paid training and certification support
- Career growth in a high-impact research setting
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What This Job Offers
Job Type
Full-time
Career Level
Senior
Education Level
No Education Listed
