Clinical Research Coordinator I

University of Chicago • Hyde Park, VT

1d

About The Position

The Clinical Research Coordinator I (CRC1) will assist the principal investigator (PI) and research team with health disparities research studies, including those related to sickle cell disease. This will primarily consist of screening and enrolling patients for studies, as well as study logistics, data collection, and data entry into REDCap. The General Internal Medicine (GIM) section at the University of Chicago has a strong tradition in medical education and research, with faculty recognized as national leaders in medical ethics, health economics and policy, health services, and outcomes research.

Requirements

• A college or university degree in a related field.
• Knowledge and skills developed through < 2 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 communicate with tact and diplomacy.
• Strong organizational skills.
• Strong communication skills (verbal and written).
• Excellent interpersonal skills.
• Strong data management skills and attention to detail.
• 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.

Nice To Haves

• Bachelor's degree.
• Knowledge of medical terminology/environment.
• Knowledge of Microsoft Word, Excel and Adobe Acrobat.

Responsibilities

• Screen and enroll patients.
• Communicate with clinical teams and community partners.
• Coordinate lab testing as needed for consented patients.
• Assist with literature searches.
• Assist with manuscript preparation and presentations.
• Lead monthly study team meetings.
• Present research updates in weekly lab meetings.
• Collect data electronically and on paper.
• Enter data into REDCap database.
• Coordinate and may participate in quality assurance reviews conducted by study sponsors, federal agencies, or specially designated review groups.
• Analyze study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports.
• Accountable for all tasks in basic clinical studies.
• Uses knowledge of clinical studies to coordinate the collection of analyzable clinical research data and/or samples.
• Performs other related work as needed.

Benefits

• Health benefits
• Retirement benefits
• Paid time off

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Number of Employees: 5,001-10,000 employees