Nephrology Clinical Research Coordinator - Full-Time

Cincinnati Children's Office of Academic Affairs and Career Development; Cincinnati (OH); On-site; USD 52,000 - 76,000; Full time

Job summary

Cincinnati Children’s Office of Academic Affairs and Career Development is seeking a Clinical Research Coordinator to support study conduct, regulatory submissions, and participant recruitment in a nephrology setting. The role emphasizes collaboration with investigators, sponsors, and clinical teams across regulatory and data-management tasks.

The candidate will maintain study records, ensure compliance, and train staff as needed, with a focus on data integrity and participant safety in a

Qualifications

• Bachelor's degree required in a related field.
• 1+ years of related experience OR Master's degree in related field.
• Knowledge of statistical process control principles.

Responsibilities

• Study Conduct/ Clinical Research Practice - Maintain awareness of status of all active studies. Arrange for facilities and supplies. Ensure participant and study compliance, i.e. collection of study specimens, and study visits.
• Regulatory Compliance and Documentation - Prepare, submit & maintain all regulatory submissions accurately & within a timely manner. Oversee review/approval of human research protocols.
• Recruitment/Enrollment/Retention - Identify potential participants and maintain tracking system for enrollment.
• Communication - Communicate with investigators, sponsors, coordinating centers, study coordinators, clinical and research teams.
• Data Management - Create CRFs, enter data, perform data quality checks and maintain records.

Skills

Statistical process control

Education

Bachelor's degree in a related field

Master's degree in a related field

Job description

Cincinnati Children’s Office of Academic Affairs and Career Development is seeking a Clinical Research Coordinator to support study conduct, regulatory submissions, and participant recruitment in a nephrology setting. The role emphasizes collaboration with investigators, sponsors, and clinical teams across regulatory and data-management tasks.

The candidate will maintain study records, ensure compliance, and train staff as needed, with a focus on data integrity and participant safety in a