U

University of Chicago

Private research university in Chicago, IL

Clinical Trials Monitor

Full-TimeUpdated on 10/4/2026Deadline 2/3/27
$65k - $80k
Mid, Senior
Bachelor's
Chicago, IL, USA
HybridHybrid work includes remote data review and onsite monitoring visits at Hyde Park Campus.

About the job

Requirements
  • A college or university degree in a related field is required.
  • Knowledge and skills developed through 2–5 years of work experience in a related job discipline are required.
  • Ability to interact and communicate clearly, tactfully, and courteously with patrons, patients, staff, faculty, students, and others.
  • Strong organizational skills are required.
  • Strong data management skills and attention to detail are required.
  • Knowledge of the Microsoft Suite, including Outlook, is required.
  • Ability to understand complex documents, such as clinical trials, is required.
  • Ability to handle competing demands with diplomacy and enthusiasm is required.
  • Ability to absorb large amounts of information quickly is required.
  • Adaptability to changing working situations and work assignments is required.
Responsibilities
  • Ensure clinical research compliance with federal, state, and local regulations and University of Chicago Comprehensive Cancer Center regulations and policies.
  • Administer required monitoring tasks as outlined in monitoring plans and in compliance with applicable regulations.
  • Monitor through remote data review and onsite visits at Hyde Park Campus; work remotely and in person as required.
  • Manage multiple projects while working independently and in a team environment.
  • Ensure Principal Investigators and study teams adhere to current FDA regulations, applicable ICH/GCP guidelines, local policies, and standard operating procedures, including monitoring standards and guidelines.
  • 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, meeting timelines for completing monitoring activities and submitting written monitoring reports.
  • 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.
  • Account for all tasks in moderately complex clinical studies.
  • Assist with professional, organizational, and operational tasks under moderate supervision.
  • Perform other related work as needed.
Desired Qualifications
  • A bachelor's degree is preferred.
  • Three years of progressively responsible clinical trials experience is strongly preferred.
  • One year of monitoring experience is strongly preferred.
  • Five years of University or academic medicine administrative experience is strongly preferred.
  • Strong interpersonal skills are preferred.

About the company

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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