Clinical Research Coordinator (CRC) – Phase I–IV Trials

UCI group; Irvine (CA); On-site; USD 43,000 - 61,000; Full time

Job summary

UC Irvine is seeking Temporary Full-Time Clinical Research Coordinators for positions at the UCI Medical Center in Orange and the UCI campus in Irvine. Responsibilities include coordinating Phase I–IV trials, screening participants, and ensuring data quality and regulatory compliance.

Applicants should have 3–5 years CRC experience, strong data management skills, and the ability to work with study teams. English proficiency is required; bachelor’s degree preferred.

Qualifications

• Knowledge of clinical research processes, including trial coordination and human subject research regulations.
• 3-5 years previous experience as a clinical research coordinator (CRC).
• 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.

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.

Skills

Clinical research processes

CRC experience 3–5 years

Data management

Protocol compliance

Communication & organization

English fluency

Education

Bachelor's degree or equivalent

Job description

UC Irvine is seeking Temporary Full-Time Clinical Research Coordinators for positions at the UCI Medical Center in Orange and the UCI campus in Irvine. Responsibilities include coordinating Phase I–IV trials, screening participants, and ensuring data quality and regulatory compliance.

Applicants should have 3–5 years CRC experience, strong data management skills, and the ability to work with study teams. English proficiency is required; bachelor’s degree preferred.