Senior Clinical Research Coordinator – Pediatric Trials

Cincinnati Children's Office of Academic Affairs and Career Development; Cincinnati (OH); On-site; USD 57,000 - 62,000; Full time

Job summary

Cincinnati Children’s is seeking qualified Clinical Research Coordinators (CRCs) to support vivacious translational and clinical research programs. You will coordinate participant recruitment, enrollment, and study visits, while ensuring regulatory compliance and accurate data handling across multiple studies.

The role emphasizes collaboration with multidisciplinary teams on the Burnet Campus in Cincinnati, with strong emphasis on Good Clinical Practice and participant safety.

Qualifications

• Bachelor's degree in science/health fields or related area, with relevant work experience.
• Experience in human subjects research or clinical studies is preferred.
• Strong organization and communication skills with attention to detail.
• Proficiency with Microsoft Office applications (Word/Excel/PowerPoint).

Responsibilities

• Coordinate day-to-day research study activities.
• Recruit, screen, consent, and retain study participants.
• Schedule and conduct study visits and follow-up activities.
• Maintain regulatory documents and study records.
• Manage regulatory submissions and approvals.
• Enter and validate data in electronic databases.
• Collect and process specimens as needed for studies.
• Collaborate with investigators, sponsors, and clinical teams.
• Support study monitoring visits, audits, and quality assurance.

Skills

Strong organizational skills

Communication skills

Problem-solving

Microsoft Office

Education

Bachelor's degree in a scientific, healthcare, public health, psychology, or related field

Master's degree

Tools

REDCap

Medidata

OnCore

Job description

Cincinnati Children’s is seeking qualified Clinical Research Coordinators (CRCs) to support vivacious translational and clinical research programs. You will coordinate participant recruitment, enrollment, and study visits, while ensuring regulatory compliance and accurate data handling across multiple studies.

The role emphasizes collaboration with multidisciplinary teams on the Burnet Campus in Cincinnati, with strong emphasis on Good Clinical Practice and participant safety.