Senior Clinical Research Coordinator (CRC) Knowledge Research Center Orange, CA Job Details Full-time $72,000 - $80,000 a year 17 hours ago Benefits Health insurance Dental insurance 401(k) Paid time off Vision insurance Life insurance Qualifications Spanish English High school diploma or GED Research project coordination ICH guidelines Clinical data entry Data entry Research regulatory compliance Productivity software Clinical quality assurance standards FDA regulations Full Job Description About Us Knowledge Research Center is a growing clinical research site dedicated to advancing medicine through high-quality clinical trials. We specialize in Gastroenterology, Hepatology, Metabolic Disease, Obesity, and other therapeutic areas. Our team is committed to excellence, regulatory compliance, and providing exceptional care to our research participants. Position Summary We are seeking an experienced Senior Clinical Research Coordinator (CRC) to join our team. The ideal candidate is highly organized, detail-oriented, and capable of independently managing multiple Phase II-IV clinical trials from study start-up through closeout while ensuring compliance with

GCP, FDA

regulations, and sponsor requirements. This position requires a motivated professional who enjoys working in a fast-paced environment and takes pride in delivering high-quality clinical research. Responsibilities Coordinate and manage multiple clinical research studies simultaneously. Recruit, screen, consent, and enroll study participants. Conduct study visits according to protocol requirements. Collect, process, and ship laboratory specimens. Perform ECGs, vital signs, and other protocol-required procedures. Maintain accurate source documentation and electronic case report forms (eCRFs). Ensure protocol compliance and participant safety. Schedule subject visits and maintain study timelines. Prepare for sponsor monitoring visits, audits, and inspections. Resolve data queries promptly. Maintain regulatory documentation and essential study files. Communicate effectively with sponsors, CROs, vendors, and investigators. Assist with study feasibility, site initiation, and closeout activities. Mentor and support junior coordinators and research staff.

Qualifications Required:

Minimum 3+ years of Clinical Research Coordinator experience. Experience coordinating industry-sponsored clinical trials. Strong knowledge of

ICH-GCP, FDA

regulations, and clinical research processes. Excellent organizational and time-management skills. Strong written and verbal communication skills. Ability to multitask and work independently. Proficiency with electronic data capture (EDC) systems and Microsoft Office. High school diploma or equivalent (Associate's or Bachelor's degree preferred). Fluent in

English and Spanish Preferred:

Experience with Gastroenterology, Hepatology, MASH/MASLD/NASH, Obesity, or Internal Medicine studies. Experience with CRIO or other electronic source documentation systems. Phlebotomy experience. IATA and GCP certifications.

Pay:

$72,000.00 - $80,000.00 per year

Benefits:

401(k) Dental insurance Health insurance Life insurance Paid time off Vision insurance

Work Location:

In person