Pediatric Clinical Research Coordinator II

Cincinnati Children's Hospital Medical Center; United States; On-site; USD 51,000 - 59,000; Full time

Job summary

Cincinnati Children's is seeking Clinical Research Coordinators II to support studies that advance child health across multiple departments. You will work with investigators, participants, and teams to ensure studies run safely, efficiently, and in compliance with regulations.

Responsibilities include coordinating daily activities, recruiting and scheduling participants, maintaining study data, and supporting IRB submissions.

Qualifications

• High School Diploma and two (2) years of related work experience OR Bachelor's degree in a related field.
• Strong organizational and time management skills.
• Excellent communication and interpersonal skills.
• Attention to detail and accuracy.
• Professionalism and accountability.

Responsibilities

• Coordinating day-to-day research study activities.
• Recruiting, screening, scheduling, and retaining study participants.
• Supporting informed consent and participant education activities.
• Collecting, entering, and maintaining study data and documentation.
• Maintaining regulatory files and research records.
• Assisting with IRB submissions and compliance activities.
• Communicating with participants, families, investigators, and study teams.
• Monitoring study progress and ensuring protocol adherence.
• Supporting quality assurance and regulatory compliance efforts.

Skills

Organizational skills

Time management

Communication skills

Interpersonal skills

Attention to detail

Adaptability

Teamwork

Education

High School Diploma

Bachelor's degree

Job description

Cincinnati Children's is seeking Clinical Research Coordinators II to support studies that advance child health across multiple departments. You will work with investigators, participants, and teams to ensure studies run safely, efficiently, and in compliance with regulations.

Responsibilities include coordinating daily activities, recruiting and scheduling participants, maintaining study data, and supporting IRB submissions.