Nephrology Clinical Research Coordinator - Impactful Trials

Cincinnati Children's Hospital Medical Center; Cincinnati (OH); On-site; USD 42,000 - 66,000; Full time

Job summary

Cincinnati Children’s is seeking a Clinical Research Coordinator in Nephrology to support study conduct, regulatory compliance, participant recruitment, and data management. You will collaborate with investigators, monitor study activities, ensure protocol adherence, and maintain study documentation across multiple trials.

This role requires attention to detail, strong organization, and effective communication with sponsors and clinical teams.

Qualifications

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

Responsibilities

• Study Conduct/Clinical Research Practice: Maintain awareness of status of all active studies; arrange facilities and supplies; ensure participant and study compliance; train staff in collection, processing and labeling of samples; ensure proper logging and storage of specimens.
• Regulatory Compliance and Documentation: Prepare, submit & maintain regulatory submissions; participate in audits and quality reviews; ensure regulatory requirements are met and documented; maintain accurate records.
• Recruitment/Enrollment/Retention: Identify potential participants, maintain tracking, conduct pre-consent screening, obtain informed consent, coordinate with clinical teams, track enrollment, address recruitment challenges.
• Communication: Oversee study correspondence; liaise with internal and external stakeholders; ensure smooth communication about study issues.
• Data Management: Create CRFs, ensure data quality, perform data cleaning, maintain databases, generate reports.

Skills

Statistical process control

Education

Bachelor's degree in related field

Job description

Cincinnati Children’s is seeking a Clinical Research Coordinator in Nephrology to support study conduct, regulatory compliance, participant recruitment, and data management. You will collaborate with investigators, monitor study activities, ensure protocol adherence, and maintain study documentation across multiple trials.

This role requires attention to detail, strong organization, and effective communication with sponsors and clinical teams.