Clinical Research Coordinator II/III — Elite Trials & Data

CO00 Children's Hospital Medical Center

United States

On-site

USD 51,000 - 64,000

Full time

2 days ago

Be an early applicant

Application generator

Don’t send a generic resume — generate a resume and cover letter tailored to this exact role.

Get past ATS filters

Job summary

Cincinnati Children’s is seeking a Biomedical Research Coordinator at the CRC II/CRC III level to support behavioral medicine/clinical psychology research. The role involves coordinating studies, preparing regulatory documents, recruiting families, and ensuring data quality and compliance with GCP and IRB requirements.

The position requires relevant education and experience with a strong emphasis on ethics, participant safety, and accurate documentation.

Qualifications

Requires CRC II: High school diploma or equivalent plus 2 years of related work experience.
CRC III requires Bachelor's in a related field and 1 year related work experience, or a Master's in a related field.

Responsibilities

Coordinate clinical research studies by preparing personnel and materials, drafting protocols and informed consent forms for IRB review.
Assemble lab kits and collect/store samples as per SOPs and study instructions.
Ensure regulatory documents are current, assist with SOPs, IRB filings, and regulatory communications.
Approach potential participants, conduct pre-consent screening, obtain informed consent, and document enrollment.
Maintain accurate data: complete Case Report Forms, source docs, and data entry in auditable systems.
Assist with audit readiness and ensure Good Clinical Practice compliance.