Pediatric All of Us Research Coordinator

University of Kansas Medical Center; Kansas City (KS); On-site; USD 61,000 - 91,000; Full time

Benefits offered by this job

Comprehensive benefits package

Day-one health benefits

Job summary

University of Kansas Medical Center is seeking a Clinical Research Coordinator for the All of Us Research Program within Internal Medicine. The role coordinates pediatric enrollment, biospecimen collection, data documentation, and protocol compliance across KU Health System sites and community centers.

You will support participant engagement and collaborate with investigators and healthcare staff. Key duties include educating participants, screening eligibility, managing CRFs, and reporting to

Qualifications

• Four (4) years of experience in health sciences, nursing, or related field.
• Two (2) years clinical research experience.
• Experience with CFR, GCP, and HIPAA.
• Experience interpreting regulatory guidance and requirements.

Responsibilities

• Educate participants, evaluate eligibility, and recruit families for the research program.
• Conduct recruitment outreach at community events and enrollment locations.
• Maintain source documents and submit case report forms (CRFs).
• Recognize and report adverse events to supervisor, PI, FDA, and sponsors.
• Perform protocol-required procedures including biospecimen collection and processing.
• Maintain study supplies and participate in monitoring visits and audits.
• Provide written and verbal reports to the PI and senior leadership.
• Ensure compliance with GCP guidelines and FDA regulations.

Skills

Organization

Problem solving

Communication

Computer skills

Multi-tasking

Job description

University of Kansas Medical Center is seeking a Clinical Research Coordinator for the All of Us Research Program within Internal Medicine. The role coordinates pediatric enrollment, biospecimen collection, data documentation, and protocol compliance across KU Health System sites and community centers.

You will support participant engagement and collaborate with investigators and healthcare staff. Key duties include educating participants, screening eligibility, managing CRFs, and reporting to