Clinical Research Coordinator III, Various Departments

• Expected Starting Pay Range $56,784.00 - $62,150.40
• Starting pay is based on experience, skills, and equity; exceptions may apply for highly qualified candidates. Additional pay (e.g., shift, on‑call, or weekend differentials) and benefits may apply. Annual pay may vary based on FTE status.

Burnet Campus

Pediatrics / CCRF Admin

Day (United States of America)

Full time

40

1

Regular

• Expected Starting Pay Range $56,784.00 - $62,150.40
• Starting pay is based on experience, skills, and equity; exceptions may apply for highly qualified candidates. Additional pay (e.g., shift, on‑call, or weekend differentials) and benefits may apply. Annual pay may vary based on FTE status.

Cincinnati Children's is seeking talented Clinical Research Coordinators (CRCs) 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. CRCs may coordinate participant recruitment and enrollment, conduct study visits, manage regulatory documentation, collect and process research specimens, oversee study data, collaborate with multidisciplinary teams, and ensure compliance with research protocols and regulatory requirements.

Please note, this is an onsite position located in Cincinnati, Ohio.

• Oncology
• Cardiology
• Pulmonary Medicine
• Gastroenterology
• Neurology
• Behavioral Health
• Emergency Medicine
• Population Health
• Genomic Medicine
• Translational Research
• Biorepository and Specimen-Based Research

Specific responsibilities, study complexity, and required experience will vary by position.

• 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

• 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
• Strong organizational, communication, and problem-solving skills
• Ability to manage multiple priorities while maintaining attention to detail
• Proficiency with Microsoft Office applications

• Human subjects research
• Participant recruitment and enrollment
• Clinical trials or observational research
• Regulatory submissions and compliance
• Research data management
• Electronic data capture systems (REDCap, Medidata, OnCore, or similar)
• Specimen processing and biobanking
• Healthcare, patient-facing, or clinical environments
• Good Clinical Practice (GCP) training

As part of the application process, candidates may be asked to complete a brief questionnaire and/or one-way video interview to help us better understand their research experience, areas of expertise, and career interests. This information allows our recruitment team to match candidates with the most appropriate CRC opportunities across the organization.

At Cincinnati Children's, we come to work with one goal: to make children's health better. We believe in a holistic team approach, both in caring for patients and their families, and in…