Senior Clinical Research Coordinator (CRC)
Share
Job Location:
Yearly Salary:
Experience Required:
Posted on:
30+ days ago
Vacancies:
1 Vacancy
Job Summary
Job description
Job Title: Senior Clinical Research Coordinator (Liver Trials)
Job Type: Full-Time On-Site
Job Location: Orange CA
Job Salary: $90000-$100000 per year (based on experience)
Industry: Clinical Research Hepatology Phase I IV Trials
About Us:
We re a fast-paced compliance-driven research clinic specializing in liver disease trials from NASH and cirrhosis to hepatocellular carcinoma. Our team 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.
MUST HAVE - Experience in CRC in Liver/GI/Obesity studies
Key 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
Requirements
Qualifications
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
Bilingual (Spanish/English) preferred
Familiarity with California specific regulations
Certifications
GCP Training (Required)
HIPAA & Human Subjects Protection (Required)
CPHS Compliance Training (Required)
CCRC (Certified Clinical Research Coordinator) (Preferred)
CCRP (Certified Clinical Research Professional) (Preferred)
Benefits
Competitive salary performance bonuses
Health dental and vision coverage
Paid training and certification support
Career growth in a high-impact research setting
Qualifications 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 Bilingual (Spanish/English) preferred Familiarity with California specific regulations
Education
Qualifications (Required): Bachelor's degree in health sciences 3-5+ year clinical research experience Certifications: GCP Training (Required) HIPAA & Human Subjects Protection (Required) CPHS Compliance Training (Required) CCRC (Certified Clinical Research Coordinator) (Preferred) CCRP (Certified Clinical Research Professional) (Preferred)
Company Industry
Biotechnology Research / Pharmaceutical Manufacturing
Key Skills
- CSS
- Cloud Computing
- Health Education
- Actuary
- Building Electrician
