UC Irvine
Temporary Clinical Research Coordinator (CRC)
UC Irvine, Irvine, California, United States, 92713
Temporary Clinical Research Coordinator (CRC)
2 days ago Be among the first 25 applicants
About UC Irvine Founded in 1965, UC Irvine is a member of the prestigious Association of American Universities and is ranked among the nation’s top 10 public universities by U.S. News & World Report. The campus has produced five Nobel laureates and is known for its academic achievement, premier research, innovation and anteater mascot. Led by Chancellor Howard Gillman, UC Irvine has more than 36,000 students and offers 224 degree programs. It’s located in one of the world’s safest and most economically vibrant communities and is Orange County’s second-largest employer, contributing $7 billion annually to the local economy and $8 billion statewide. To learn more about UC Irvine, visit www.uci.edu.
Your Role on the Team
The incumbent is responsible for coordinating clinical trials, including comprehensive coordination and data management of complex phase I‑IV clinical research protocols from initiation through completion.
The incumbent will conduct interviews with study patients in the clinic, screen participants, and collect data in compliance with established study protocols.
Develop and establish a process for review and oversight of clinical trials conducted by investigators, ensuring study protocols are followed, appropriate documentation is kept, and accurate data is collected according to Good Clinical Practice (GCP), internal SOPs, and University policies.
Complete timely and accurate collection and coordination of data submission to study sponsors, ensuring quality control and timely milestone payments.
Compile and transcribe research patient data and study‑related information into case report forms (CRFs) and sponsor‑specific electronic data capture systems (EDC).
Work with the clinical research team to manage and collect accurate data and assist Principal Investigators and study coordinators for all data‑management aspects.
Clinical research offices and clinics are located at the UCI Medical Center in Orange and the UCI campus in Irvine, as well as various community sites throughout Orange County; the incumbent will be required to work at both main locations and, when necessary, at community sites.
Required Qualifications
Minimum of 3 years of related work experience as a clinical research coordinator (CRC) or assistant CRC with a Bachelor’s degree or equivalent experience.
Demonstrated track record of human subjects research (Phase I–III drug trials and device trials) coordination, informed consent procedures, and IRB submissions.
Experience working in a medical/clinical setting and familiarity with medical terminology.
Bachelor’s degree in a related area or equivalent combination of education and/or experience.
May require study‑management coordination outside normal business hours.
May require travel to off‑site research locations.
Must possess and maintain a valid California driver’s license; subject to the California DMV’s “Pull Notice System” and continued employment contingent on satisfactory driving record.
Preferred Qualifications
SOCRA or ACRP certification.
Salary and Benefits Pay Rate: $33.08 per hour.
Benefits may include medical insurance, sick and vacation time, retirement savings plans, and access to discounts and perks. For more information on compensation practices and benefits, please visit our benefits page.
Employment Conditions Applicants must comply with the following conditions of employment: Background check and Live Scan; Employment Misconduct; legal right to work in the United States; vaccination policies; smoking and tobacco policy; drug‑free environment; final administrative or judicial decisions regarding misconduct within the last seven years; California Child Abuse and Neglect Reporting Act; E‑Verify; pre‑placement health evaluation. Temporary employment may require a health physical or valid California driver’s license for university vehicles. Hours are Monday–Friday 8:00 a.m.–5:00 p.m., with occasional part‑time, weekend, and evening hours available.
Equal Opportunity Employer Statement The University of California is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected categories covered by the UC Anti‑Discrimination Policy. We are committed to attracting and retaining a diverse workforce and honoring unique experiences, perspectives, and identities. Reasonable accommodations for applicants with disabilities are available upon request. For more information, contact Human Resources at (949) 824‑0500 or eec@uci.edu.
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About UC Irvine Founded in 1965, UC Irvine is a member of the prestigious Association of American Universities and is ranked among the nation’s top 10 public universities by U.S. News & World Report. The campus has produced five Nobel laureates and is known for its academic achievement, premier research, innovation and anteater mascot. Led by Chancellor Howard Gillman, UC Irvine has more than 36,000 students and offers 224 degree programs. It’s located in one of the world’s safest and most economically vibrant communities and is Orange County’s second-largest employer, contributing $7 billion annually to the local economy and $8 billion statewide. To learn more about UC Irvine, visit www.uci.edu.
Your Role on the Team
The incumbent is responsible for coordinating clinical trials, including comprehensive coordination and data management of complex phase I‑IV clinical research protocols from initiation through completion.
The incumbent will conduct interviews with study patients in the clinic, screen participants, and collect data in compliance with established study protocols.
Develop and establish a process for review and oversight of clinical trials conducted by investigators, ensuring study protocols are followed, appropriate documentation is kept, and accurate data is collected according to Good Clinical Practice (GCP), internal SOPs, and University policies.
Complete timely and accurate collection and coordination of data submission to study sponsors, ensuring quality control and timely milestone payments.
Compile and transcribe research patient data and study‑related information into case report forms (CRFs) and sponsor‑specific electronic data capture systems (EDC).
Work with the clinical research team to manage and collect accurate data and assist Principal Investigators and study coordinators for all data‑management aspects.
Clinical research offices and clinics are located at the UCI Medical Center in Orange and the UCI campus in Irvine, as well as various community sites throughout Orange County; the incumbent will be required to work at both main locations and, when necessary, at community sites.
Required Qualifications
Minimum of 3 years of related work experience as a clinical research coordinator (CRC) or assistant CRC with a Bachelor’s degree or equivalent experience.
Demonstrated track record of human subjects research (Phase I–III drug trials and device trials) coordination, informed consent procedures, and IRB submissions.
Experience working in a medical/clinical setting and familiarity with medical terminology.
Bachelor’s degree in a related area or equivalent combination of education and/or experience.
May require study‑management coordination outside normal business hours.
May require travel to off‑site research locations.
Must possess and maintain a valid California driver’s license; subject to the California DMV’s “Pull Notice System” and continued employment contingent on satisfactory driving record.
Preferred Qualifications
SOCRA or ACRP certification.
Salary and Benefits Pay Rate: $33.08 per hour.
Benefits may include medical insurance, sick and vacation time, retirement savings plans, and access to discounts and perks. For more information on compensation practices and benefits, please visit our benefits page.
Employment Conditions Applicants must comply with the following conditions of employment: Background check and Live Scan; Employment Misconduct; legal right to work in the United States; vaccination policies; smoking and tobacco policy; drug‑free environment; final administrative or judicial decisions regarding misconduct within the last seven years; California Child Abuse and Neglect Reporting Act; E‑Verify; pre‑placement health evaluation. Temporary employment may require a health physical or valid California driver’s license for university vehicles. Hours are Monday–Friday 8:00 a.m.–5:00 p.m., with occasional part‑time, weekend, and evening hours available.
Equal Opportunity Employer Statement The University of California is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected categories covered by the UC Anti‑Discrimination Policy. We are committed to attracting and retaining a diverse workforce and honoring unique experiences, perspectives, and identities. Reasonable accommodations for applicants with disabilities are available upon request. For more information, contact Human Resources at (949) 824‑0500 or eec@uci.edu.
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