Senior Pediatric Clinical Research Coordinator

Cincinnati Children's Hospital Medical Center; Cincinnati (OH); On-site; USD 57,000 - 62,000; Full time

Job summary

Cincinnati Children's Hospital Medical Center is seeking talented Clinical Research Coordinators to support innovative clinical and translational research programs across a wide range of specialties, playing a critical role in advancing discoveries that improve child health.

This onsite role is located in Cincinnati, Ohio and will involve coordinating participant recruitment, study visits, regulatory documentation, and data management.

Qualifications

• Bachelor's degree in a scientific, healthcare, public health, psychology, or related field AND at least one year of related work experience OR a Master's degree.

Responsibilities

• Coordinating day-to-day research study activities
• Recruiting, screening, consenting, and retaining study participants
• Scheduling and conducting study visits
• Maintaining research records and source documentation
• Managing regulatory submissions and study approvals
• Entering and validating study data in electronic databases
• Collecting, processing, and shipping research specimens
• Collaborating with investigators, sponsors, clinical teams, and research participants
• Supporting study monitoring visits, audits, and quality assurance activities
• Ensuring compliance with protocols, institutional policies, Good Clinical Practice (GCP), and regulatory requirements

Skills

Organizational skills

Communication skills

Problem-solving

Attention to detail

Education

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

Master's degree

Tools

Microsoft Office

REDCap

Medidata

OnCore

Job description

Cincinnati Children's Hospital Medical Center is seeking talented Clinical Research Coordinators to support innovative clinical and translational research programs across a wide range of specialties, playing a critical role in advancing discoveries that improve child health.

This onsite role is located in Cincinnati, Ohio and will involve coordinating participant recruitment, study visits, regulatory documentation, and data management.