Clinical research co-ordinators conduct clinical trials for medical world. They are responsible for ensuring that the trials are conducted in an ethical manner, referring to a good clinical practice. They majorly work under Clinical Research Managers (CRM) and are allocated with the administering clinical trials. The primary roles and responsibilities of CRC comprise of managing clinical trials, collecting data, informing participants about study objectives, and administering questionnaires. Also clinical research co-ordinators are ‘the organizers’ in the research lab. They enable quality clinical trials which are completed with only selected subjects, organized information, and accurate reports. Co-ordinators make it possible for the great strides made in the medical world by offering accurate proof of medical advances found in clinical trials in all areas from basic preventive care to curing diseases, and everything in between. Additionally, CCRC is granted to a CRC meeting the q
