Clinical Research Coordinator – Pediatric Oncology Registry

Cincinnati Children's Office of Academic Affairs and Career Development; Cincinnati (OH); On-site; USD 34,000 - 36,000; Full time

Job summary

Join Cincinnati Children’s Oncology research team as a Clinical Research Coordinator to support the International DIPG Registry. You will coordinate with sites across the U.S. and internationally, support registry operations, manage data requests, and contribute to multiple registry-based projects within pediatric oncology research.

This role emphasizes collaboration, organization, and attention to regulatory and data-management details to advance meaningful pediatric cancer research.

Qualifications

• CRC II requires a high school diploma and 2 years of related work experience.
• CRC III requires a Bachelor's degree in a related field and 1 year of experience or a Master's degree.

Responsibilities

• Coordinate studies, prepare protocols and consent documents for IRB review.
• Maintain regulatory records and assist with regulatory filings.
• Identify eligible participants and coordinate study visits.
• Organize study communications and support cross-team collaboration.
• Complete CRFs and data entry, ensuring data quality and traceability.

Skills

CRC coordination

IRB management

Data management

Recruitment

Communication

Education

High school diploma

Bachelor's degree

Job description

Join Cincinnati Children’s Oncology research team as a Clinical Research Coordinator to support the International DIPG Registry. You will coordinate with sites across the U.S. and internationally, support registry operations, manage data requests, and contribute to multiple registry-based projects within pediatric oncology research.

This role emphasizes collaboration, organization, and attention to regulatory and data-management details to advance meaningful pediatric cancer research.