Clinical Research Coordinator II/III: Study Operations

Cincinnati Children's Office of Academic Affairs and Career Development

Cincinnati (OH)

On-site

USD 51,000 - 55,000

Full time

19 hours ago
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Job summary

Cincinnati Children’s is seeking staff to support clinical research activities within Behavioral Med-Clin Psychology. The role supports study conduct, regulatory compliance, recruitment, and data management across multiple studies conducted in a pediatric setting.

Responsibilities include preparing IRB documents, coordinating participant visits, and ensuring data integrity in electronic systems while maintaining study-wide communication with the clinical team.

Qualifications

  • High school diploma or equivalent with 2 years related experience.
  • Bachelor's degree in a related field preferred.
  • CRC III requires Bachelor's degree with 1 year experience or Master's degree.

Responsibilities

  • Coordinate study conduct by preparing materials and documents for IRB/sponsor review.
  • Assemble lab kits, collect and label samples, and ensure proper storage.
  • Identify regulatory activities and maintain accurate records.
  • Recruit and enroll participants, conduct pre-consent screening, and document processes.
  • Complete CRFs and enter data into auditable systems; perform data quality checks.

Skills

Clinical research coordination
Regulatory compliance
Participant recruitment
Data management

Education

High school diploma or equivalent
Bachelor's degree in related field
Master's degree in related field

Tools

CRFs
Electronic data capture systems

Job description

Cincinnati Children’s is seeking staff to support clinical research activities within Behavioral Med-Clin Psychology. The role supports study conduct, regulatory compliance, recruitment, and data management across multiple studies conducted in a pediatric setting.

Responsibilities include preparing IRB documents, coordinating participant visits, and ensuring data integrity in electronic systems while maintaining study-wide communication with the clinical team.

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