Clinical Research Coordinator II – Oncology Trials

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

Job summary

University of Chicago in Chicago, IL seeks a Clinical Research Coordinator2 to support daily clinical trial activities under supervision. The role partners with the PI and research management to coordinate compliance, data collection, and study operations across multiple trials.

The CRC2 will manage screening, enrollment, consent processes, data entry, and coordination with sponsors, CROs, and regulatory bodies to ensure adherence to protocols and federal guidelines.

Qualifications

• College or university degree in related field required.
• 2–5 years of work experience in a related job discipline.

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 principal investigators, research team members, sponsors, CROs, and regulatory authorities related to the conduct of a clinical trial.
• 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.

Skills

Written communication

Oral communication

Condense complex information

Education

College or university degree in related field

Bachelor's degree

Job description

University of Chicago in Chicago, IL seeks a Clinical Research Coordinator2 to support daily clinical trial activities under supervision. The role partners with the PI and research management to coordinate compliance, data collection, and study operations across multiple trials.

The CRC2 will manage screening, enrollment, consent processes, data entry, and coordination with sponsors, CROs, and regulatory bodies to ensure adherence to protocols and federal guidelines.