Full-Time

Clinical Trials Monitor

Updated on 9/3/2026

Deadline 2/3/27
University of Chicago

University of Chicago

Private research university in Chicago, IL

Compensation Overview

$65k - $80k/yr

Chicago, IL, USA

Hybrid

Hybrid work includes remote data review and on-site monitoring visits at the Hyde Park Campus.

Bachelor's

Category
Biology & Biotech (1)
Required Skills
Microsoft Outlook

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Requirements
  • A college or university degree in a related field.
  • Knowledge and skills developed through 2–5 years of work experience in a related job discipline.
  • Ability to interact and communicate with clarity, tact, and courtesy with patrons, patients, staff, faculty, students, and others.
  • Ability to work remotely and in person.
  • Ability to work independently and in a team environment.
Responsibilities
  • Ensure compliance of clinical research with federal, state, and local regulations and University of Chicago Comprehensive Cancer Center regulations and policies.
  • Administer required monitoring tasks as outlined in the monitoring plan and in compliance with applicable regulations.
  • Monitor through a combination of remote data review and on-site monitoring visits at the Hyde Park Campus.
  • Manage multiple projects concurrently while meeting monitoring timelines.
  • Ensure Principal Investigators and study teams adhere to current Food and Drug Administration regulations, applicable International Council for Harmonisation Good Clinical Practice guidelines, local policies, and standard operating procedures.
  • Adhere to the UCCCC Data Safety Monitoring Plan, including monitoring visit type, frequency, and required critical monitoring activities, using monitoring tracking forms and related tools and templates.
  • Support protocol start-up activities.
  • Independently coordinate upcoming and ongoing monitoring assignments and submit written monitoring reports within expected timelines.
  • Assist in developing and writing clinical trial monitoring plans.
  • Provide recommendations and guidance to study-specific monitoring teams and assist with audit readiness and preparation.
  • Be accountable for all tasks in moderately complex clinical studies.
  • Assist with professional, organizational, and operational tasks under moderate supervision.
Desired Qualifications
  • A Bachelor's degree.
  • 3 years of progressively responsible clinical trials experience.
  • 1 year of monitoring experience.
  • 5 years of University or academic medicine administrative experience.
  • Knowledge of the Microsoft Suite, including Outlook.
  • Strong organizational skills.
  • Strong interpersonal skills.
  • Strong data management skills and attention to detail.
  • Ability to understand complex documents such as clinical trials.
  • Ability to handle competing demands with diplomacy.
  • Ability to absorb large amounts of information quickly.
  • Adaptability to changing working situations and work assignments.
University of Chicago

University of Chicago

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The University of Chicago is a private research university founded in 1890 in Chicago's Hyde Park neighborhood. It comprises the College, graduate divisions, and professional schools across a broad range of disciplines.

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