Clinical Research Coordinator: Lead Phase I–IV Trials

UC Irvine; Irvine (CA); On-site; USD 51,000 - 55,000; Full time

Job summary

UC Irvine is seeking Temporary Full-Time Clinical Research Coordinators for its medical center and campus sites. You will coordinate Phase I–IV trials, screen and enroll participants, and ensure data integrity across CRFs and EDC systems.

Required are 3–5 years of CRC experience, strong data management skills, and familiarity with GCP and study protocols. English proficiency and effective communication are essential for coordinating with teams and participants.

Qualifications

• 3–5 years' experience as a clinical research coordinator.

Responsibilities

• Coordinate and manage Phase I-IV clinical trials from initiation through closeout.

Skills

Clinical coordination

Data management

Regulatory knowledge

Communication skills

English proficiency

Education

Bachelor's degree or equivalent

Tools

EDC systems

Clinical databases

Job description

UC Irvine is seeking Temporary Full-Time Clinical Research Coordinators for its medical center and campus sites. You will coordinate Phase I–IV trials, screen and enroll participants, and ensure data integrity across CRFs and EDC systems.

Required are 3–5 years of CRC experience, strong data management skills, and familiarity with GCP and study protocols. English proficiency and effective communication are essential for coordinating with teams and participants.