"Temporary Clinical Research Coordinator (CRC)"

University of California Irvine

Temporary Clinical Research Coordinator (CRC)

Req ID: 145975

Payroll Job Title: 009335-CLIN RSCH CRD

Location: Irvine, California

Organization: UCI Campus

Division: Campus Administration

Department: Temporary Employment Services

Position Type: Full Time

Salary Range Minimum: USD $33.08/Hr.

Salary Range Maximum: USD $54.51/Hr.

Who We Are

Founded in 1965, UC Irvine is a member of the prestigious Association of American Universities and is ranked among the nation's top 10 public universities by U.S. News & World Report. The campus has produced five Nobel laureates and is known for its academic achievement, premier research, innovation and anteater mascot. Led by Chancellor Howard Gillman, UC Irvine has more than 36,000 students and offers 224 degree programs. It's located in one of the world's safest and most economically vibrant communities and is Orange County's second-largest employer, contributing $7 billion annually to the local economy and $8 billion statewide.

To learn more about UC Irvine, visit www.uci.edu.

Your Role on the Team

This recruitment is for Temporary Full-Time Clinical Research Coordinator positions through UCI's internal temporary staffing service. Clinical research offices and clinics are located at the UCI Medical Center in Orange and the UCI campus in Irvine, as well as various clinics at community sites throughout Orange County.

Job duties include, but are not limited to:

• Coordinate and manage Phase I-IV clinical trials from initiation through closeout, ensuring compliance with study protocols and timelines.
• Screen, interview, and enroll study participants; collect and document clinical data in accordance with established protocols.
• Oversee data management activities, including accurate entry into case report forms (CRFs) and electronic data capture (EDC) systems.
• Ensure adherence to Good Clinical Practice (GCP), internal SOPs, and university policies through ongoing monitoring and documentation oversight.

What It Takes to be Successful

Required:

• Knowledge of clinical research processes, including trial coordination and human subject research regulations.
• Strong data management skills with attention to accuracy and detail in documentation and reporting.
• Ability to interpret and follow complex study protocols and regulatory requirements (e.g., GCP).
• Effective communication and organizational skills to coordinate with research teams and study participants.
• Ability to read, write, and follow written and oral instructions in English.

Preferred:

• Experience supporting Phase I-IV clinical trials in an academic or healthcare setting.
• Familiarity with electronic data capture (EDC) systems and clinical research databases.
• Experience working with Principal Investigators and cross-functional research teams.
• Ability to develop and improve processes for study oversight and compliance.

Total Compensation

In addition to the salary range listed below, we offer a wealth of benefits to make working at UCI even more rewarding. These benefits may include medical insurance, sick and vacation time, retirement savings plans, and access to a number of discounts and perks. Please utilize the links listed here to learn more about our compensation practices and benefits.

$35.77/hour (within range of $35.77/hour - $36.54/hour)