Senior Clinical Research Coordinator — Complex Trials Lead

Cincinnati Children's Office of Academic Affairs and Career Development

Cincinnati (OH)

On-site

USD 61,000 - 78,000

Full time

4 days ago
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Job summary

Cincinnati Children's, Allergy Department, Burnet Campus, is seeking a Clinical Research Coordinator for a full-time day shift. This 40-hour FTE position supports complex multi-center studies under the PI, with collaboration across divisions to ensure compliant trial conduct.

The role emphasizes regulatory oversight, data management, recruitment, and staff training to ensure high-quality research outcomes and proper specimen handling.

Qualifications

  • Bachelor's degree in a related field.
  • 3+ years of experience in related job discipline OR a related Master's with 2 years experience.
  • Cert Clinical Research Coord within 18 months of external hire.

Responsibilities

  • Study Conduct/Clinical Research Practice: serve as a resource for all aspects of conducting a clinical trial for complex and multi-center trials under the PI; supervise staff and train new personnel.
  • Regulatory Compliance and Documentation: coordinate regulatory activities, prepare submissions, audits, and ensure accuracy and timeliness of records.
  • Recruitment/Enrollment/Retention: oversee recruitment plans, track enrollment, identify barriers, and maintain participant tracking systems.
  • Data Management: oversee data entry/validation, create CRFs, maintain data dictionaries, and ensure data quality and reporting.

Skills

3+ years of experience

Education

Bachelor's degree in a related field
Cert Clinical Research Coord within 18 months

Job description

Cincinnati Children's, Allergy Department, Burnet Campus, is seeking a Clinical Research Coordinator for a full-time day shift. This 40-hour FTE position supports complex multi-center studies under the PI, with collaboration across divisions to ensure compliant trial conduct.

The role emphasizes regulatory oversight, data management, recruitment, and staff training to ensure high-quality research outcomes and proper specimen handling.

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