Administration

Clinical Research Coordinator | Orange, CA & Mission Viejo, CA | Temp-to-Perm

This is a temporary-to-permanent Clinical Research Coordinator opportunity with a hybrid work option. The role floats between two outpatient locations in Orange, CA, and Mission Viejo, CA. Candidates should be within a reasonable commute of both sites.

Schedule: Monday–Friday, Days (8:00 AM–5:00 PM)

Contract Duration: 13 weeks, with permanent hire potential

Clinical Scope:

This role supports multiple active clinical research studies with a patient-facing focus, primarily serving cardiology and stroke patient populations. Responsibilities include:

• Consenting study participants and managing ongoing participation compliance
• Performing vitals and EKGs; processing and shipping biological samples
• Dispensing investigational product (IP) with full accountability documentation
• Entering visit data into electronic data capture systems within required timelines
• Coordinating with Principal Investigators, study sponsors, and the IRB
• Maintaining regulatory files, study binders, and protocol compliance per GCP/ICH guidelines
• Recruiting and retaining study participants

Note: No blood draws are required. Device management trials and bench/data-only trial experience are not applicable to this role — patient-facing clinical trials experience is required.

Required Qualifications:

• Minimum 2 years of patient-facing clinical research experience (consenting, vitals, labs, medication dispensing, documentation)
• Strong proficiency in Microsoft Office (Outlook, Teams, Word, Excel)
• CCRC (ACRP) certification preferred

A plus:

• Cardiology or oncology research background
• Spanish or Korean language skills

Float between both designated outpatient sites is required. Refusal to float may impact assignment status.