Clinical Research Coordinator II/III - Study Operations

CO00 Children's Hospital Medical Center; United States; On-site; USD 51,000 - 62,000; Full time

Job summary

Cincinnati Children’s Hospital Medical Center in Cincinnati, OH, is seeking a Clinical Research Coordinator II/III to support study conduct, regulatory compliance, and data management in the Hospital Medicine division. Responsibilities include coordinating study activities, managing regulatory documents, and ensuring accurate data capture.

The role involves direct interaction with participants, adherence to GCP/SOPs, and collaboration with investigators, sponsors, and the clinical team.

Qualifications

• CRC II requires high school diploma or equivalent and 2 years of related work experience.
• CRC III requires Bachelor's degree in a related field and 1 year of related work experience, or a Master's degree in a related field.
• Starting Salary Range: CRC II: 24.46 – 26.23/hr; CRC III: 56,784.00 - 62,150.40 annually

Responsibilities

• Coordinate studies by preparing personnel and materials and documents for IRB review.
• Assemble lab kits, collect and label samples, and ensure proper storage.
• Maintain regulatory documentation, SOPs, and audit readiness support.
• Enter data and complete Case Report Forms per GCP and SOPs.
• Communicate with participants and clinical team per protocol.

Education

High school diploma or equivalent

Bachelor's degree in a related field

Job description

Cincinnati Children’s Hospital Medical Center in Cincinnati, OH, is seeking a Clinical Research Coordinator II/III to support study conduct, regulatory compliance, and data management in the Hospital Medicine division. Responsibilities include coordinating study activities, managing regulatory documents, and ensuring accurate data capture.

The role involves direct interaction with participants, adherence to GCP/SOPs, and collaboration with investigators, sponsors, and the clinical team.