Clinical Research Coordinator: Drive Trials & Compliance

Cincinnati Children's; Cincinnati (OH); On-site; USD 57,000 - 80,000; Full time

Job summary

Cincinnati Children's in Cincinnati, OH, is seeking a Clinical Research Coordinator to manage study conduct across multiple active protocols in the Allergy department. You will ensure participant safety, oversee regulatory submissions, assist with recruitment, and maintain essential trial documentation.

The role requires coordinating with investigators, sponsors and clinical teams to support compliant study execution.

Qualifications

• Bachelor's degree in a related field with 1 year of directly related work experience, or a Master's degree in a related field
• Bachelor's degree in a related field with 3 years of related experience or Master's degree with 2 years; CRC certification within 18 months

Responsibilities

• Study Conduct/ Clinical Research Practice: monitor active studies, arrange facilities, ensure compliance, train staff on specimen handling and SOPs
• Regulatory Compliance and Documentation: prepare submissions, audits, monitor visits, ensure regulatory approvals and record keeping
• Recruitment/Enrollment/Retention: identify potential participants, screen, consent, track enrollment, report progress
• Communication: maintain correspondence, liaise with departments, sponsors, and sites
• Data Management: create CRFs, enter data accurately, perform data cleaning and generate reports
• Support data-management and respond to queries from sponsors, statisticians, and project team

Education

Bachelor's degree in a related field with 1 year of directly related work experience, or a Master's degree in a related field

Bachelor's degree in a related field with 3 years of related experience or Master's degree with 2 years; CRC certification within 18 months

Job description

Cincinnati Children's in Cincinnati, OH, is seeking a Clinical Research Coordinator to manage study conduct across multiple active protocols in the Allergy department. You will ensure participant safety, oversee regulatory submissions, assist with recruitment, and maintain essential trial documentation.

The role requires coordinating with investigators, sponsors and clinical teams to support compliant study execution.