Oncology Clinical Trials Coordinator — Research Operations

University of Chicago; Chicago (IL); On-site; USD 65,000 - 85,000; Full time

Job summary

University of Chicago Comprehensive Cancer Center (UCCCC) seeks a Clinical Research Coordinator 2 (CRC2) to partner with the PI and manage daily trial activities under supervision. You will handle enrollment, data collection, and regulatory tasks, ensuring protocol adherence and patient safety.

You will coordinate visits, assist with informed consent, IRB submissions, and data integrity, supporting a high-volume trial program in the BSD. Strong communication with sponsors and staff is essential.

Qualifications

• Experience coordinating clinical trials and managing regulatory tasks.
• Ability to recruit and screen study participants under PI guidance.
• Familiarity with IRB processes and study start-up activities.

Responsibilities

• Manages all aspects of conducting clinical trials including screening, enrollment, follow-up, case report forms, and adverse event reports.
• Recruits and interviews potential study patients with guidance from PI and staff.
• Collects, processes, ships and stores specimens according to aseptic techniques.
• Coordinates study startup through closeout, including informed consent and protocol adherence.
• Ensures patient data confidentiality and compliance with regulations.

Skills

Clinical Research Coordination

Patient Recruitment

Regulatory Compliance

IRB Submissions

Data Management

Job description

University of Chicago Comprehensive Cancer Center (UCCCC) seeks a Clinical Research Coordinator 2 (CRC2) to partner with the PI and manage daily trial activities under supervision. You will handle enrollment, data collection, and regulatory tasks, ensuring protocol adherence and patient safety.

You will coordinate visits, assist with informed consent, IRB submissions, and data integrity, supporting a high-volume trial program in the BSD. Strong communication with sponsors and staff is essential.