Senior Clinical Research Coordinator – Pediatric Trials

Cincinnati Children's; Cincinnati (OH); On-site; USD 50,000 - 64,000; Full time

Job summary

Cincinnati Children’s is seeking a Clinical Research professional to support CRC II/III functions. You will assist in study coordination, regulatory documentation, recruitment, and data management in a pediatric clinical research setting.

The role involves preparing materials for IRB reviews, maintaining regulatory binders, coordinating visits, and ensuring compliant data entry across systems in alignment with GCP and SOPs.

Qualifications

• CRC II requires high school diploma and 2 years of related work experience.
• Preferred: Bachelor's degree in a related field.
• CRC III requires a Bachelor's or Master's degree in a related field.

Responsibilities

• Assist in coordinating studies by preparing personnel and materials, and documents for IRB/sponsor review.
• Assemble lab kits and gather supplies; collect, label, and process samples per SOPs.
• Identify regulatory activities; maintain records and assist with audits and regulatory binder.
• Coordinate recruitment, screen participants, obtain informed consent per GCP and policies.
• Complete CRFs and source docs; enter data and support data-management tasks.

Education

High school diploma or equivalent

Bachelor's degree in related field

Master's degree in related field

Job description

Cincinnati Children’s is seeking a Clinical Research professional to support CRC II/III functions. You will assist in study coordination, regulatory documentation, recruitment, and data management in a pediatric clinical research setting.

The role involves preparing materials for IRB reviews, maintaining regulatory binders, coordinating visits, and ensuring compliant data entry across systems in alignment with GCP and SOPs.