Clinical Research Coordinator II
On-site · Columbus, Ohio, United States
Job Summary
Manages elements of a clinical study to meet protocol obligations under ICH/GCP; coordinates start-up, launch, day-to-day management, and study closure; trains/mentors CRCs; recruits, consents, and enrolls subjects; ensures regulatory compliance and subject safety; coordinates subject visits, data collection, CRF completion, and regulatory binders; supports recruitment plans and study publications; requires Associate's degree or equivalent experience with CRA/CRC certification preferred and ~18 months clinical research experience.
Required Qualifications
- Associate's degree or equivalent work-related experience, required
- BA/BS, preferred
- CRA/CRC certification, preferred
- Eighteen months experience in clinical research or health care field, required
- Licensure not specified
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