Temporary Clinical Research Coordinator (CRC)
About The Position
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.
Requirements
- 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.
Nice To Haves
- 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.
Responsibilities
- 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.
Benefits
- medical insurance
- sick and vacation time
- retirement savings plans
- access to a number of discounts and perks
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
No Education Listed
Number of Employees
11-50 employees
