Clinical Research Coordinator II, Various Departments
About The Position
Cincinnati Children's is building a talent community of motivated individuals interested in Clinical Research Coordinator II opportunities across a variety of research specialties and departments. By applying to this evergreen posting, you will be considered for current and future Clinical Research Coordinator II openings throughout the organization. Qualified applicants may receive a follow-up screening questionnaire and/or brief one-way video interview after applying. This additional step helps us learn more about your experience and interests and match you with opportunities that best fit your background. Whether you're a recent graduate or have experience in healthcare, customer service, education, social services, community outreach, or another related field, we'd love to hear from you. Clinical Research Coordinators play an important role in supporting studies that improve child health through scientific discovery and innovation. Working closely with investigators, research participants, and multidisciplinary teams, Clinical Research Coordinators help ensure research studies are conducted safely, efficiently, and in compliance with applicable regulations and institutional requirements. Research opportunities may be available across a variety of specialty areas, including: Behavioral Health, Cardiology, Emergency Medicine, Gastroenterology, Genetics and Genomic Medicine, Neurology, Oncology, Population Health, Pulmonary Medicine, Rare Disease Research, Translational Research. Specific responsibilities and study assignments will vary based on departmental needs and individual positions.
Requirements
- High School Diploma and two (2) years of related work experience OR Bachelor's degree in a related field
Nice To Haves
- Bachelor's degree in life sciences, psychology, public health, health sciences, sociology, neuroscience, or a related field
- Experience in healthcare, research, customer service, education, social services, community outreach, or other participant-facing environments
- Experience coordinating projects, schedules, documentation, or administrative processes
- Experience working with patients, families, customers, clients, students, or community members
- Demonstrated ability to learn new systems, processes, and regulations
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 Institutional Review Board (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
- Learning and applying research policies, procedures, and federal regulations
Benefits
- Additional pay (e.g., shift, on‑call, or weekend differentials) and benefits may apply.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
High school or GED
