Elemental IRB
Ethics, faster.
Log In Sign Up
← Back to Glossary
Glossary Term

Clinical Research Coordinator (CRC)

Clinical Operations

Also known as: CRC, study coordinator, research coordinator

The site staff member responsible for day-to-day coordination of a clinical study under the PI's supervision.

CRCs handle screening and enrollment, source documentation, data entry, regulatory binder maintenance, monitor visits, and subject scheduling. They often serve as the primary point of contact between site, sponsor/CRO, and IRB.

Need IRB review for your study?

Elemental IRB provides fast, transparent ethical oversight for commercial and academic research.

See pricing →   How it works →