Full-Time

Clinical Research Coordinator

IPH

Posted on 8/17/2026

Deadline 8/17/27
University of California - Irvine

University of California - Irvine

Research university in Irvine, CA

Compensation Overview

$37.56 - $42.55/hr

No H1B Sponsorship

Irvine, CA, USA

In Person

Bachelor's

Category
Biology & Biotech (1)
Required Skills
Data Science
Machine Learning
Electronic Health Records (EHR)
HIPAA

Get referred to University of California - Irvine

See people who can refer or advise you

Requirements
  • Attention to detail, strong interpersonal skills, effective verbal and written communication, and the ability to multitask in a fast-paced environment.
  • Ability to work independently, complete projects in a timely manner, and prioritize multiple projects to meet deadlines.
  • Fluency in the Committee on Human Research online iMEDris system for protocol submission, renewal, and modification.
  • Understanding of the patient population sufficient to build rapport and determine realistic and appropriate patient participation.
  • Experience with electronic medical records and REDCap.
  • Knowledge of location-specific and departmental policies for reimbursement, research guidelines, confidentiality, and HIPAA regulations.
  • Experience applying Good Clinical Practice Guidelines, HIPAA, protections for human research subjects, CHR recruitment and consent regulations, effective cash-handling procedures, Environmental Health and Safety training, and Fire Safety training.
  • High school graduation and sufficient experience and demonstrated skills to perform the assigned duties and responsibilities.
  • One to three years of experience in a research environment.
Responsibilities
  • Execute, manage, and coordinate research protocols under the direction of the Assistant Director of the Institute for Precision Health.
  • Coordinate data collection and operations for several concurrent human-subjects research studies.
  • Draft and maintain Institutional Review Board submissions, manage consent processes, and coordinate sample and data collection from external and internal sources.
  • Support the management and coordination of tasks for single or multiple research studies.
  • Act as an intermediary between services and departments while overseeing data and specimen management.
  • Manage and report study results.
  • Create, clean, update, and manage databases, comprehensive datasets, and reports.
  • Assist with training Assistant Clinical Research Coordinators and assist the Clinical Research Supervisor or Principal Investigator with oversight of other research staff.
  • Manage investigator protocols in the Committee on Human Research online system, including protocol renewals, modifications, and implementation of new studies.
  • Participate in reviewing and writing protocols to obtain Institutional Review Board approval and ensure university compliance.
  • Help ensure compliance with relevant regulatory agencies.
  • Oversee study data integrity and implement and maintain periodic quality-control procedures.
  • Interface with departments to obtain UCI approval before study initiation.
  • Maintain regulatory documents.
  • Report study progress to investigators.
  • Participate in internal and external audits or reviews of study protocols.
Desired Qualifications
  • Bachelor's degree in a related field.
University of California - Irvine

University of California - Irvine

View

University of California - Irvine is a public research university in Irvine, California. It offers undergraduate, graduate, and professional education across its schools and academic programs.

Company Size

N/A

Company Stage

N/A

Total Funding

N/A

Headquarters

N/A

Founded

N/A

Get referred to University of California - Irvine

See people who can refer or advise you