Clinical Research Coordinator – Phase I–IV Trials

UC Irvine; Irvine, Northern (CA, KY); Hybrid; USD 44,000 - 63,000; Full time

Job summary

UC Irvine is seeking a Temporary Full-Time Clinical Research Coordinator to support Phase I–IV trials at the UCI Medical Center in Orange and the Irvine campus. You will screen, enroll participants and ensure data quality under GCP and study protocols.

Responsibilities include coordinating trials from initiation to closeout, managing CRFs and EDC data, and maintaining thorough regulatory documentation. Strong English communication and meticulous record-keeping are essential.

Qualifications

• Knowledge of clinical research processes and regulations.
• 3–5 years experience as a clinical research coordinator.
• Strong data management and attention to accuracy in documentation and reporting.
• Ability to interpret and follow study protocols and regulatory requirements (GCP).
• Effective communication and organizational skills for coordinating with research teams and participants.
• Proficiency in reading/writing English.

Responsibilities

• Coordinate and manage Phase I–IV clinical trials from initiation through closeout.
• Screen, interview, and enroll study participants; collect and document clinical data.
• Oversee data management activities, including entry into CRFs and EDC systems.
• Ensure adherence to GCP, SOPs, and university policies through monitoring and documentation.

Skills

Clinical research

Trial coordination

GCP compliance

Data management

English proficiency

Communication skills

Documentation accuracy

Education

Bachelor's degree or equivalent

Tools

EDC systems

Job description

UC Irvine is seeking a Temporary Full-Time Clinical Research Coordinator to support Phase I–IV trials at the UCI Medical Center in Orange and the Irvine campus. You will screen, enroll participants and ensure data quality under GCP and study protocols.

Responsibilities include coordinating trials from initiation to closeout, managing CRFs and EDC data, and maintaining thorough regulatory documentation. Strong English communication and meticulous record-keeping are essential.