The site-side operator who runs the trial day-to-day with patients and PI.
Also known as: CRC · Study Coordinator · Research Nurse Coordinator
CRCs sit at the investigator site (hospital, clinic, academic center) and are the operational owner of one or more studies. They consent participants, schedule visits, collect specimens, complete eCRFs, and interface with the monitoring CRA. Common entry point into clinical research from nursing, medical, or life-science backgrounds.
We can place a verified candidate in 2 weeks, with the dossier you actually need to make the call.