Senior Clinical Research Coordinator

Cincinnati Children's; Cincinnati (OH); On-site; USD 57,000 - 64,000; Full time

Job summary

Cincinnati Children’s is seeking a Clinical Research Professional to support multiple studies at the Burnet Campus. The role involves study conduct, regulatory submissions, participant recruitment, and robust data handling as part of a collaborative research team.

Responsibilities include ensuring protocol compliance, maintaining records for regulatory authorities, organizing enrollment tracking, and coordinating with investigators and clinical staff to advance ongoing trials.

Qualifications

• Bachelor's degree in a related field is required.
• 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 active studies, arrange facilities, ensure compliance, train staff, log specimens, and support regulatory needs.
• Regulatory Compliance and Documentation: prepare submissions, ensure audit-readiness, participate in monitor visits, ensure compliance with rules and policies; document activities.
• Recruitment/Enrollment/Retention: identify participants, manage enrollment tracking, pre-consent screening, inform consent, communicate with clinical teams, and overcome recruitment barriers.
• Communication: craft correspondence, liaise between departments, investigators, sponsors, and clinicians; maintain study-related relations.
• Data Management: create CRFs, ensure accuracy and completeness, manage data entry, validation, and reporting of study data.

Skills

Clinical Research

Regulatory Compliance

Recruitment & Retention

Communication

Data Management

Education

Bachelor's degree in a related field

Master's degree in a related field

Job description

Cincinnati Children’s is seeking a Clinical Research Professional to support multiple studies at the Burnet Campus. The role involves study conduct, regulatory submissions, participant recruitment, and robust data handling as part of a collaborative research team.

Responsibilities include ensuring protocol compliance, maintaining records for regulatory authorities, organizing enrollment tracking, and coordinating with investigators and clinical staff to advance ongoing trials.