Gastroenterology Clinical Research Coordinator II

The University Of Chicago; Chicago (IL); On-site; USD 60,000 - 75,000; Full time

Job summary

The University of Chicago is seeking a Clinical Research Coordinator II for Gastroenterology to manage all aspects of clinical trials in a high‑volume setting. You will screen, enroll, follow up with subjects, and ensure accurate data entry and adverse event reporting under the direction of the PI and CRC Manager.

Responsibilities include coordinating study startup through closeout, obtaining informed consent, scheduling procedures, and educating patients about study procedures, risks, and

Qualifications

• Minimum requirements include a college or university degree in related field.

Responsibilities

• Manages all aspects of conducting clinical trials including screening, enrollment, subject follow-up, completion of the case report form, and adverse event reports.
• Recruits and interviews potential study patients with guidance from PI and other clinical research staff.
• Collects, processes, ships and stores specimens to appropriate laboratory according to established aseptic techniques.
• Identifies and explains responsibilities of investigators, research team members, sponsors, CROs, and regulatory authorities related to clinical trials.
• Coordinates the conduct of the study from startup through closeout including recruitment and screening of study subjects, obtaining informed consent, collecting research data, and ensuring protocol adherence.
• Plans and coordinates patient schedule for study procedures, return visits, and study treatment schedules.
• Educates patients about study procedures, visit schedules, risks, and benefits.

Education

Bachelor's degree

Job description

The University of Chicago is seeking a Clinical Research Coordinator II for Gastroenterology to manage all aspects of clinical trials in a high‑volume setting. You will screen, enroll, follow up with subjects, and ensure accurate data entry and adverse event reporting under the direction of the PI and CRC Manager.

Responsibilities include coordinating study startup through closeout, obtaining informed consent, scheduling procedures, and educating patients about study procedures, risks, and