Clinical Research Coordinator: Study Ops & Compliance

Cincinnati Children's Hospital Medical Center; Cincinnati (OH); On-site; USD 42,000 - 62,000; Full time

Job summary

Cincinnati Children’s Hospital Medical Center in Cincinnati, OH is seeking a clinical research professional to support study coordination, regulatory compliance, and data management in translational and clinical pharmacology.

You will prepare protocols, consents, assemble materials, and work with IRB and sponsors; maintain records, recruit participants, and ensure GCP standards. The role offers full-time hours in a collaborative team dedicated to advancing children’s health.

Qualifications

• High school diploma or equivalent.
• 2+ years of work experience in a related job discipline or equivalent combination of education and experience.
• May require an Associate degree, vocational training, apprenticeships or equivalent.

Responsibilities

• Coordinate studies by preparing personnel and materials, preparation of protocols, informed consents, amendments and other necessary documents for review by the IRB and Sponsor.
• Assemble lab kits and/or gather supplies.
• Collect and label samples as instructed and deliver or process samples in accordance with the protocol, SOP or other work instruction set.
• Ensure specimens are properly logged, handled and stored.
• Follow direction of clinical research coordinator or others involved in the clinical research project work.
• Assist other staff members and coordinators to implement studies.
• Maintain inventory of supplies and equipment.
• Operate standard laboratory and research study equipment, if applicable.

Education

High school diploma or equivalent

2+ years of work experience in a related job discipline or equivalent combination of education and experience

Associate degree or vocational training

Job description

Cincinnati Children’s Hospital Medical Center in Cincinnati, OH is seeking a clinical research professional to support study coordination, regulatory compliance, and data management in translational and clinical pharmacology.

You will prepare protocols, consents, assemble materials, and work with IRB and sponsors; maintain records, recruit participants, and ensure GCP standards. The role offers full-time hours in a collaborative team dedicated to advancing children’s health.