UC Irvine
Temporary Assistant Clinical Research Coordinator (ACRC)
UC Irvine, Irvine, California, United States, 92713
Temporary Assistant Clinical Research Coordinator (ACRC)
Join to apply for the
Temporary Assistant Clinical Research Coordinator (ACRC)
role at
UC Irvine .
Who We Are Founded in 1965, UC Irvine is a member of the Association of American Universities, ranked among the nation’s top 10 public universities. With five Nobel laureates, a strong research culture, and more than 36,000 students, UCI is a leader in academic achievement and innovation.
Your Role on the Team This recruitment is for a Temporary Assistant Clinical Research Coordinator through UCI's internal temporary staffing service. Under the supervision of the Clinical Research Manager and the Assistant Director of Clinical Research Operations, the incumbent will coordinate clinical trials and manage data for multiple phase II–IV research protocols from initiation through completion.
Conduct patient interviews, screen participants, and collect data in compliance with study protocols.
Develop and establish processes for review and oversight of clinical trials, ensuring adherence to Good Clinical Practice (GCP), SOPs, and university policies.
Complete timely data collection and submission to study sponsors, managing quality control and milestone payments.
Compile and transcribe patient data into electronic data capture systems (EDC) and the clinical trial management system (OnCore).
Assist Principal Investigators and study coordinators with data management aspects of trials.
Maintain communication with a multilevel research network and collaborate with IRB, FDA, sponsor monitors, and other regulatory groups.
Work at UCI Medical Center in Orange, UCI campus in Irvine, and various community sites throughout Orange County as required.
What It Takes to Be Successful
Minimum 1 year of related clinical research experience.
Bachelor’s degree in a related field or equivalent combination of education and experience.
Ability to work outside normal business hours and travel to off‑site research locations.
Valid California driver’s license and compliance with the DMV Pull Notice System.
Total Compensation Pay Rate: $27.40 per hour. Benefits include medical insurance, paid time off, retirement savings plans, and other perks.
Equal Opportunity/Affirmative Action Employer The University of California, Irvine is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, or protected veteran status.
Work Authorization Sponsorship Consideration for work authorization sponsorship requires proof of eligibility to work in the United States.
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Temporary Assistant Clinical Research Coordinator (ACRC)
role at
UC Irvine .
Who We Are Founded in 1965, UC Irvine is a member of the Association of American Universities, ranked among the nation’s top 10 public universities. With five Nobel laureates, a strong research culture, and more than 36,000 students, UCI is a leader in academic achievement and innovation.
Your Role on the Team This recruitment is for a Temporary Assistant Clinical Research Coordinator through UCI's internal temporary staffing service. Under the supervision of the Clinical Research Manager and the Assistant Director of Clinical Research Operations, the incumbent will coordinate clinical trials and manage data for multiple phase II–IV research protocols from initiation through completion.
Conduct patient interviews, screen participants, and collect data in compliance with study protocols.
Develop and establish processes for review and oversight of clinical trials, ensuring adherence to Good Clinical Practice (GCP), SOPs, and university policies.
Complete timely data collection and submission to study sponsors, managing quality control and milestone payments.
Compile and transcribe patient data into electronic data capture systems (EDC) and the clinical trial management system (OnCore).
Assist Principal Investigators and study coordinators with data management aspects of trials.
Maintain communication with a multilevel research network and collaborate with IRB, FDA, sponsor monitors, and other regulatory groups.
Work at UCI Medical Center in Orange, UCI campus in Irvine, and various community sites throughout Orange County as required.
What It Takes to Be Successful
Minimum 1 year of related clinical research experience.
Bachelor’s degree in a related field or equivalent combination of education and experience.
Ability to work outside normal business hours and travel to off‑site research locations.
Valid California driver’s license and compliance with the DMV Pull Notice System.
Total Compensation Pay Rate: $27.40 per hour. Benefits include medical insurance, paid time off, retirement savings plans, and other perks.
Equal Opportunity/Affirmative Action Employer The University of California, Irvine is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, or protected veteran status.
Work Authorization Sponsorship Consideration for work authorization sponsorship requires proof of eligibility to work in the United States.
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