Rheumatology Clinical Research Coordinator II/III

Cincinnati Children's; Cincinnati (OH); On-site; USD 34,000 - 36,000; Full time

Job summary

Cincinnati Children’s Rheumatology is hiring a Clinical Research Coordinator II/III to support study conduct, regulatory compliance, recruitment, and data management under GCP and IRB guidelines. You will collaborate with clinicians, coordinate visits, prepare consent materials, and ensure accurate documentation and reporting while maintaining participant safety and protocol adherence.

CRC II requires a high school diploma with experience; CRC III requires a bachelor’s or master’s in a related

Qualifications

• High school diploma or equivalent with relevant experience for CRC II; Bachelor's degree or higher for CRC III.
• Experience coordinating clinical studies and familiarity with GCP/IRB processes preferred.
• Ability to manage regulatory documents and ensure accurate data entry.

Responsibilities

• Study conduct/coordination: prepare materials, protocols, consents; assemble lab kits; collect and label samples.
• Regulatory compliance: maintain records, prepare regulatory binder, support audits, ensure compliance with regulations.
• Recruitment/enrollment: identify eligible participants, coordinate visits, obtain informed consent.
• Communication: organize correspondence, liaise with investigators, sponsors, and teams.
• Data management: complete CRFs, enter data, perform quality checks, address data queries.

Skills

Study coordination

Regulatory compliance

Recruitment & enrollment

Data management

Communication

Education

High school diploma or equivalent

Bachelor's degree or higher

Tools

IRB submission tools

Electronic data capture (EDC) systems

Job description

Cincinnati Children’s Rheumatology is hiring a Clinical Research Coordinator II/III to support study conduct, regulatory compliance, recruitment, and data management under GCP and IRB guidelines. You will collaborate with clinicians, coordinate visits, prepare consent materials, and ensure accurate documentation and reporting while maintaining participant safety and protocol adherence.

CRC II requires a high school diploma with experience; CRC III requires a bachelor’s or master’s in a related