Clinical Research Coordinator II - Gastroenterology Trials

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 to partner with the clinical PI and Clinical Research Manager in the Gastroenterology Section. The role involves coordinating all phases of clinical trials, ensuring protocol adherence, and maintaining data integrity.

You will screen and enroll participants, obtain informed consent, manage data and specimen handling, and liaise with sponsors, CROs, and regulatory authorities to ensure compliance and patient safety.

Qualifications

• Education requirements include a college degree.
• Experience in coordinating multiple clinical trials is preferred.
• Familiarity with IRB submissions and regulatory processes.

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.
• 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 to be performed, visit schedule, what to report between and during visits, and the risks and benefits of the procedures.

Skills

Clinical research

Regulatory compliance

IRB submissions

Data management

Study coordination

Education

Bachelor's degree

Job description

The University of Chicago is seeking a Clinical Research Coordinator II to partner with the clinical PI and Clinical Research Manager in the Gastroenterology Section. The role involves coordinating all phases of clinical trials, ensuring protocol adherence, and maintaining data integrity.

You will screen and enroll participants, obtain informed consent, manage data and specimen handling, and liaise with sponsors, CROs, and regulatory authorities to ensure compliance and patient safety.