Cardiology Clinical Research Coordinator — Impactful Trials

University of Illinois Chicago; Chicago (IL); On-site; USD 60,000 - 90,000; Full time

Benefits offered by this job

Health insurance

Dental insurance

Vision insurance

Life Insurance

Retirement plan

Paid time off

Tuition waivers

Job summary

University of Illinois Chicago is seeking a Clinical Research Coordinator in Cardiology to support multiple patient-centered trials. The role involves coordinating regulatory, enrollment, and follow-up activities under the Division of Cardiology leadership.

The ideal candidate holds a health-related Bachelor's degree and has 1–2 years of coordination experience. Familiarity with IRB submission, informed consent, and GCP is preferred. Benefits accompany this position.

Qualifications

• Bachelor's degree in a health-related field required.
• 1–2 years clinical research coordination experience preferred.
• Familiarity with IRB submission processes, informed consent, and GCP preferred.

Responsibilities

• Coordinate regulatory, enrollment, and follow-up activities for each study with Cardiology PIs.
• Prepare and submit IRB applications, informed consent documents, and trial agreements.
• Screen patients for eligibility and obtain consent per protocol.
• Enroll and randomize patients per protocol.
• Maintain research records and regulatory files for sponsor and institution.
• Serve as liaison between division, sponsors, monitors, and during sponsor visits.

Skills

Regulatory coordination

Enrollment & consent

Trial coordination

Education

Bachelor's degree in health-related field

Tools

IRB software

Job description

University of Illinois Chicago is seeking a Clinical Research Coordinator in Cardiology to support multiple patient-centered trials. The role involves coordinating regulatory, enrollment, and follow-up activities under the Division of Cardiology leadership.

The ideal candidate holds a health-related Bachelor's degree and has 1–2 years of coordination experience. Familiarity with IRB submission, informed consent, and GCP is preferred. Benefits accompany this position.