Clinical Trials Monitor
$65,000–$80,000 year
HybridChicago, Illinois, United States
Job Summary
Manage and monitor daily clinical research activities for moderately complex studies, ensuring compliance with federal, state, local, and University regulations. Administer monitoring tasks including remote data review and onsite visits to verify adherence to FDA guidelines, ICH/GCP standards, and standard operating procedures. Coordinate upcoming and ongoing assignments while independently developing monitoring plans and preparing audit-ready documentation. Provide recommendations to study teams and support protocol start-up activities across the University's extensive clinical trials program. Hybrid work arrangements are utilized for onsite monitoring visits in Hyde Park.
Required Qualifications
- college or university degree in related field
- 2-5 years of work experience in a related job discipline
- willingness and ability to work remotely and in person
- strong time management skills
- ability to work independently and in a team environment
- knowledge and skills developed through 2-5 years of work experience in a related job discipline
Desired Qualifications
- 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
- Ability to interact and communicate with clarity, tact, and courtesy with patrons, patients, staff, faculty, students, and others
- Strong organizational skills
- Excellent interpersonal skills
- Strong data management skills and attention to detail
- Knowledge of the Microsoft Suite, including Outlook
- Ability to understand complex documents (e.g., clinical trials)
- Ability to handle competing demands with diplomacy and enthusiasm
- Ability to absorb large amounts of information quickly
- Adaptability to changing working situations and work assignments
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