Administration

Clinical Research Coordinator — Orange, CA

This is a temporary-to-permanent Clinical Research Coordinator role supporting patient-facing clinical trials in oncology, cardiology, and stroke. The position is hybrid-eligible and floats between two outpatient locations in Orange and Mission Viejo, CA.

Schedule & Contract

• Days, 5×8-hour shifts (8:00 AM – 5:00 PM)
• 13-week contract with permanent conversion potential

What You'll Do

• Oversee day-to-day operations of multiple concurrent clinical research studies
• Serve as the primary liaison between the Principal Investigator, patients, sponsors, and the IRB
• Obtain informed consent, perform vitals and EKGs, dispense investigational product, and process labs
• Ensure timely and accurate data entry into electronic data capture systems (within 7 days of visit)
• Manage investigational product accountability, including temperature monitoring and return/destruction
• Recruit, consent, and retain study participants; coordinate appointments and study-required labs
• Process, package, and ship biological samples per study protocol
• Maintain participant binders and perform regulatory functions for active studies

Requirements

• Minimum 2 years of patient-facing clinical research coordination experience (consenting, vitals, EKGs, lab processing, data entry, medication dispensing)
• Patient-facing trials required; device management or bench/data-only trials experience not accepted
• Cardiology or stroke experience a plus
• CCRC (ACRP) preferred
• Strong proficiency in Microsoft Office (Outlook, Teams, Word, Excel)
• Spanish or Korean language skills a plus

Float: Travel between two Southern California outpatient sites is required.