Clinical Research Coordinator - 16965-1A
Updated: Apr 5, 2021
Location: UC Irvine Campus
Department: UCI Ctr for Clinical Research
Job Opening ID: 16965Reports To: Clinical Research SupervisorWorking Title: Clinical Research CoordinatorDepartment: UCI Ctr for Clinical ResearchBargaining Unit: RXFLSA: Non-ExemptPayroll Job Code: 009335Job Location: UCI Campus - IrvinePercent of Time: 100%Work Schedule: 8-5, M-FEmployee Class: Career Position Summary: Under the supervision of the Clinical Research Supervisor of the Center for Clinical Research (CCR), incumbent is responsible for coordinating clinical trials in the UCI Center for Clinical Research. Responsible for all aspects of clinical research 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. Incumbent will develop and establish process for review and oversight of clinical trials conducted by investigators and will ensure study protocols are followed, appropriate documentation is kept, and accurate data is collected. Incumbent will be responsible for recruiting patients onto various studies. Consents and communicates with the patient to ensure they have full understanding of the protocol (time commitment, purpose of study, risks, benefits, compliance, etc. Functions as resource to advise principal investigators, RNs, technicians and other staff to accurately implement protocol parameters and be compliant with Good Clinical Practices (GCP).
Obtain and record medical data according to clinical research protocols; may require patient interviews and screening, contact referring physicians and hospitals, and abstracting from medical records and reports.
Ensures all HIPAA policies and procedures for research and human subjects are followed. Coordinate Site Initiation Visit when new protocols are open and oversee compliance with all clinical research procedures across departments. Compensation Range: Hourly: $29.11 - $37.39 Department Website: http://clinicalresearch.som.uci.edu Required:
- 3-5 years’ work experience with a BA/BS or equivalent experience.Demonstrated track record of human subject’s 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 gastroenterology terminology. Ability to establish and maintain effective working relationships with all levels of campus and hospital administration staff, faculty, and industry sponsors. Proficient in MS Word, Excel, and PowerPoint. Ability to independently compose correspondence, design spreadsheets and design databases. Good communication skills both oral and written. Ability to use proper English grammar and spelling. Excellent organizational skills: ability to prioritize, handle multiple tasks concurrently, and function under time constraints. Demonstrated evidence of successful multi-tasking and complex problem-solving abilities. Ability to work after-hours and occasional weekends.
- SoCRA or ACRP Certified. Previous UC system experience. Experience working with IRB, PRMC, IACUC and ICTS. Knowledge of QUEST, OnCore, Kuali Financial System and Kuali Coeus. Knowledge of University IRB policies and procedures as they apply to the submission and conduct of clinical research.