Clinical Research Coordinator | Patient-Centric Study Ops

Medix™; Chicago (IL); On-site; USD 60,000 - 75,000; Full time

Job summary

Medix is seeking a Clinical Study Coordinator in Chicago to manage participant recruitment, screening, enrollment, and consent, ensuring adherence to protocol.

You will schedule visits, administer tests, monitor safety, collect data into electronic data capture systems, and coordinate with investigators, sponsors, and IRB as needed. This role emphasizes GCP compliance and clear communication with patients and team.

Qualifications

• Must have attention to detail and ability to follow protocols (≤140 chars)

Responsibilities

• Recruit, screen, and enroll patients; obtain informed consent.
• Schedule and manage study visits, administer treatments or tests, and monitor participant safety.
• Collect, record, and enter data accurately into electronic data capture systems.
• Follow Good Clinical Practice (GCP) guidelines and support IRB submissions.
• Act as a main contact for patients, investigators, sponsors, and medical staff.

Job description

Medix is seeking a Clinical Study Coordinator in Chicago to manage participant recruitment, screening, enrollment, and consent, ensuring adherence to protocol.

You will schedule visits, administer tests, monitor safety, collect data into electronic data capture systems, and coordinate with investigators, sponsors, and IRB as needed. This role emphasizes GCP compliance and clear communication with patients and team.