Smarter HR Solutions LLC·Orange, California
Lead the execution of Phase I–IV liver trials, including patient screening, enrollment, and follow-up. Manage regulatory submissions, source documentation, and oversee biospecimen handling and lab coordination.
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 I–IV Trials About Us: 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. 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.
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.
Market context
In California, Senior Clinical Research Coordinator roles are often competitive because employers look for coordinators who can manage complex protocols, patient-facing workflows, and regulatory documentation in active research settings. This posting is especially selective due to the need for 3-5+ years in liver, GI, or obesity studies, Spanish fluency, and current GCP, HIPAA, and CPHS certifications. Review the AI-summarized requirements and benefits here to quickly confirm fit and focus your application on relevant study experience and compliance credentials.