Oncology Clinical Research Coordinator - Cancer Trials

University of Illinois Chicago; Chicago (IL); On-site; USD 55,000 - 65,000; Full time

Job summary

The University of Illinois Chicago invites applications for a Clinical Research Coordinator in the Cancer Center. You will manage multiple clinical protocols, coordinate IRB submissions, and oversee patient recruitment and informed consent processes.

Your role includes data management, study coordination across sites, and collaboration with physicians, sponsors, and regulatory bodies to ensure protocol compliance and timely study progress in oncology trials.

Qualifications

• Bachelor's degree in nursing, science, or a health-related field is required.
• CCRC or Certified Clinical Research Professional certification preferred and required within 2 years of hire.
• At least one year experience in a research discipline is required.
• Experience with Federal Regulations and IRB is required; oncology research experience preferred.
• Familiarity with medical terminology and procedures including electronic medical records and billing preferred.
• Proficiency in Microsoft Office and other related software.

Responsibilities

• Coordinate and manage clinical research protocols, including pre- and post-research activities.
• Notify physicians and staff of adverse events and protocol modifications.
• Handle IRB submissions, amendments, and adverse event reports.
• Coordinate patient recruitment, screening, and enrollment to meet protocol requirements.
• Conduct informed consent process and document patient consent.
• Ensure compliance with protocols, regulatory standards, and sponsor guidelines.
• Assist in data management and preparation for reports and publications.
• Collaborate with physicians, staff, sponsors, and IRB offices across projects.

Skills

Interpersonal skills

Written and oral communication

Customer service

Office software

Education

Bachelor's degree in nursing, science, or health-related field

CCRC or Certified Clinical Research Professional certification

Tools

Electronic Medical Records

Microsoft Office

Job description

The University of Illinois Chicago invites applications for a Clinical Research Coordinator in the Cancer Center. You will manage multiple clinical protocols, coordinate IRB submissions, and oversee patient recruitment and informed consent processes.

Your role includes data management, study coordination across sites, and collaboration with physicians, sponsors, and regulatory bodies to ensure protocol compliance and timely study progress in oncology trials.