Dynamic Clinical Research Coordinator (Temporary)

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

Job summary

UC Irvine is recruiting for a Temporary Full-Time Clinical Research Coordinator to support Phase I-IV trials at UCI Medical Center in Orange and UCI campus in Irvine. The role involves coordinating trials, screening participants, data collection, and monitoring compliance with GCP and SOPs.

The position requires 3-5 years of CRC experience, strong data management skills, and excellent communication to collaborate with study teams and participants.

Qualifications

• 3-5 years CRC experience.
• Knowledge of GCP and regulatory requirements.
• Strong data management and documentation skills.
• Ability to follow study protocols and regulatory requirements.
• English language proficiency in reading/writing.

Responsibilities

• Coordinate and manage Phase I-IV clinical trials from initiation through closeout.
• Screen, recruit, and enroll participants and document data per protocols.
• Oversee data entry into CRFs and EDC systems.
• Ensure adherence to GCP, SOPs, and university policies.

Skills

CRC experience

Data management

GCP knowledge

English proficiency

Education

Bachelor's degree or equivalent

Tools

EDC systems

Job description

UC Irvine is recruiting for a Temporary Full-Time Clinical Research Coordinator to support Phase I-IV trials at UCI Medical Center in Orange and UCI campus in Irvine. The role involves coordinating trials, screening participants, data collection, and monitoring compliance with GCP and SOPs.

The position requires 3-5 years of CRC experience, strong data management skills, and excellent communication to collaborate with study teams and participants.