Temp FT Clinical Research Coordinator — Phase I–IV Trials

University of California - Irvine; Irvine (CA); On-site; USD 49,276 - 50,337; Full time

Benefits offered by this job

Medical insurance

Sick and vacation time

Retirement savings plans

Job summary

A leading public university in California is looking for a Temporary Full-Time Clinical Research Coordinator to manage and oversee clinical trials. The position requires knowledge of trial coordination and strong data management skills. You will be responsible for enrolling study participants and ensuring compliance with research protocols. Ideal candidates possess effective communication and organizational skills. A competitive hourly rate is offered, along with comprehensive benefits for temporary employees.

Qualifications

• Knowledge of trial coordination and human subject research regulations.
• Attention to accuracy and detail in documentation and reporting.
• Ability to follow written and oral instructions in English.

Responsibilities

• Coordinate and manage Phase I-IV clinical trials.
• Screen, interview, and enroll study participants.
• Ensure compliance with study protocols and Good Clinical Practice.

Skills

Knowledge of clinical research processes

Strong data management skills

Effective communication and organizational skills

Ability to interpret study protocols

Tools

Electronic data capture (EDC) systems

Job description

A leading public university in California is looking for a Temporary Full-Time Clinical Research Coordinator to manage and oversee clinical trials. The position requires knowledge of trial coordination and strong data management skills. You will be responsible for enrolling study participants and ensuring compliance with research protocols. Ideal candidates possess effective communication and organizational skills. A competitive hourly rate is offered, along with comprehensive benefits for temporary employees.