Clinical Research/Clinical Trial () RN

Title: Clinical Research Coordinator – RN II
Location: Newport Beach, CA 92663

Job Duration: 13 Weeks
Shift: 5x8 Hour Day Shifts (Monday–Friday, 8:30 AM – 5:00 PM)
Hours per Week: 40 Hours

Requirements:

• Minimum 2 years of clinical research experience
• Knowledge of GCP, FDA regulations, and human subject protection
• Strong communication and organizational skills
• Proficiency with Microsoft Office applications
• Active California RN license
• BLS certification

Preferred:

• BSN or higher
• ACRP or SoCRA certification
• Experience with IRB documentation

Schedule: Monday–Friday, 8:30 AM – 5:00 PM
Must have an active California RN license.

Job Summary:

The Clinical Research Coordinator – RN II is responsible for coordinating and managing clinical research studies, including drug, device, and biologic trials. This role works closely with physicians, sponsors, and internal teams while ensuring compliance with Good Clinical Practice (GCP), FDA regulations, and human subject protection guidelines.

Responsibilities:

• Manage industry-sponsored, government-funded, and investigator-initiated clinical trials
• Ensure compliance with GCP, FDA, and regulatory standards
• Coordinate study start-up, patient recruitment, and informed consent
• Collect, document, and maintain accurate study data and regulatory files
• Monitor and report adverse events per protocol
• Collaborate with study teams and support ongoing research activities