Clinical Research Coordinator II/III: Study Ops & Compliance

CO00 Children's Hospital Medical Center; United States; On-site; USD 54,000 - 70,000; Full time

Job summary

Cincinnati Children's is seeking Clinical Research Coordinators (CRC II/III) to support study conduct, regulatory compliance, and data management. The role emphasizes coordinating study activities, coordinating consent processes, and assisting with IRB submissions and regulatory documentation.

Salary ranges are provided for CRC II and CRC III positions. Join a leading pediatric research institution and contribute to ethical, compliant studies that advance child health.

Qualifications

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

Responsibilities

• Coordinate study conduct by preparing personnel and materials and assembling protocols and consent forms.
• Collect and label samples, maintain logs, and ensure proper storage and handling.
• Assist regulatory activities and maintain records to support IRB and sponsor requirements.
• Support participant recruitment, screening, consent, visits, and reimbursement procedures.
• Enter data and complete Case Report Forms in accordance with GCP and SOPs.

Education

High school diploma or equivalent

Bachelor's degree

Job description

Cincinnati Children's is seeking Clinical Research Coordinators (CRC II/III) to support study conduct, regulatory compliance, and data management. The role emphasizes coordinating study activities, coordinating consent processes, and assisting with IRB submissions and regulatory documentation.

Salary ranges are provided for CRC II and CRC III positions. Join a leading pediatric research institution and contribute to ethical, compliant studies that advance child health.