Clinical Research Coordinator II/III — Pediatric Impact

Cincinnati Children's; United States; On-site; USD 34,000 - 36,000; Full time

Job summary

Cincinnati Children’s is seeking a full-time Research Coordinator II/III in the Behavioral Med-Clin Psychology department in the United States. The role involves coordinating studies, ensuring regulatory compliance, enrolling participants, managing communications, and handling data management.

Salary ranges are provided for CRC II and CRC III levels. Responsibilities include coordinating visits, obtaining consent, maintaining records, and ensuring ethical standards per GCP/ICH.

Qualifications

• High school diploma or equivalent is required.
• Bachelor’s degree in a related field is preferred.
• For CRC III: Bachelor’s degree with 1 year of related experience or a Master’s degree is required.

Responsibilities

• Study Conduct/Clinical Research Practice: coordinate studies, prepare protocols and consents, assemble materials, collect and process samples, log and store specimens.
• Regulatory Compliance and Documentation: assemble materials, maintain records, ensure regulatory compliance and audit readiness.
• Recruitment/Enrollment/Retention: identify eligible participants, plan visits, provide instructions and reimbursements, obtain informed consent.
• Communication: organize correspondence, coordinate with investigators and sponsors, maintain relationships with participants.
• Data Management: complete CRFs and source documentation, ensure data accuracy, support data-management processes.

Education

High school diploma or equivalent

Bachelor’s degree in a related field

Master’s degree in a related field

Job description

Cincinnati Children’s is seeking a full-time Research Coordinator II/III in the Behavioral Med-Clin Psychology department in the United States. The role involves coordinating studies, ensuring regulatory compliance, enrolling participants, managing communications, and handling data management.

Salary ranges are provided for CRC II and CRC III levels. Responsibilities include coordinating visits, obtaining consent, maintaining records, and ensuring ethical standards per GCP/ICH.