Full-Time

Clinical Research Coordinator

Posted on 8/15/2025

Deadline 2/13/26
University of Chicago

University of Chicago

Compensation Overview

$50k - $65k/yr

+ Salary

Chicago, IL, USA

In Person

Category
Biology & Biotech (2)
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Requirements
  • Education: Minimum requirements include a college or university degree in related field.
  • Work Experience: Minimum requirements include knowledge and skills developed through < 2 years of work experience in a related job discipline.
Responsibilities
  • Plays a central role in managing all aspects of clinical trials from start-up through close-out.
  • Lead patient recruitment, coordinate study visits, and conduct informed consent discussions while ensuring protocol adherence and patient safety.
  • Oversee specimen handling, perform study assessments, manage case report forms and adverse event documentation, and safeguard patient data with meticulous attention to confidentiality and compliance.
  • Liaise with principal investigators, sponsors, CROs, and regulatory bodies, and prepare and maintain IRB submissions and approvals.
  • Training new staff, participating in audits, resolving logistical and administrative challenges, and maintaining detailed research records.
  • Accountable for all tasks in basic clinical studies.
  • Assists with various professional, organizational, and operational tasks under direct supervision.
  • Supports quality assurance reviews conducted by study sponsors, federal agencies, or specially designated review groups.
  • Uses knowledge of clinical studies to coordinate the collection of analyzable clinical research data and/or samples.
  • Performs other related work as needed.
Desired Qualifications
  • Experience in conducting oncology trials and research.
University of Chicago

University of Chicago

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