UC Irvine · 1 day ago
Temporary Clinical Research Coordinator (CRC)
Irvine, CA
Full-time
Onsite
Mid Level
$33.08/hr - $33.08/hr
3+ years expUC Irvine is a prestigious public university known for its academic achievement and research. They are seeking a Temporary Clinical Research Coordinator to coordinate clinical trials, manage data, and ensure compliance with study protocols under the supervision of the Clinical Research Manager.
Higher Education
Responsibilities
Independently or under the supervision of the Clinical Research Manager and the Assistant Director of Clinical Research Operations, the incumbent is responsible for coordinating clinical trials
Incumbent is responsible for comprehensive coordination and data management of complex phase I – IV clinical research protocols from initiation through completion of research projects with human subjects
Incumbent will conduct interviews with study patients in the clinic, screen participants, and collect data in compliance with established study protocols
Develop and establish process for review and oversight of clinical trials conducted by investigators and ensure study protocols are followed, appropriate documentation is kept, and accurate data is collected according to Good Clinical Practice (GCP), internal standard operating procedures (SOPs), and University policies and procedures
Complete timely and accurate collection and coordination of data submission to study sponsors ensuring quality control and leading to timely milestone payments
This includes responsibility for the compilation and transcription of research patient data and study-related information into case report forms (CRFs) into sponsor specific electronic data capture systems (EDC)
S/he will work with the clinical research team to manage and collect accurate data and assist Principal Investigators and study coordinators for all data management aspects
Qualification
Required
A minimum of 3 years of related work experience as a clinical research coordinator (CRC) or an assistant CRC with a Bachelor's degree or equivalent experience
Demonstrated track record of human subjects research (Phase I, II, III drug trials, and device trials) coordination, informed consent procedures and documents, and IRB submissions
Experience working in a medical/clinical setting and familiarity with medical terminology
Bachelor's degree in 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
Position is subject to the California DMV's 'Pull Notice System' and continued employment is contingent upon proof of satisfactory driving record
Preferred
SOCRA or ACRP Certification preferred
Benefits
Medical insurance
Sick and vacation time
Retirement savings plans
Access to a number of discounts and perks
Paid vacation
Holidays
Sick leave
Company
UC Irvine
UC Irvine
10001+ employees
H1B Sponsorship
UC Irvine has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (113)
2024 (86)
2023 (99)
2022 (76)
2021 (81)
2020 (79)
Funding
Current Stage
Late StageLeadership Team
Anand Gala
CEO Roundtable Member
Bob Romney
Chancellor's CEO Roundtable
Recent News
Business News: Pasadena Star-News
2025-12-29
2025-08-08
Company data provided by crunchbase