Clinical trial monitoring checks on the safety, rights, and
well-being of clinical trial subjects to ensure that they are protected. It
also checks for the data coming out of a clinical trial to be accurate and credible.
This kind of monitoring is carried out by a sponsor representatve, like the
Clinical Research Associate (CRA) by visiting a clinical trial site in person
at regular intervals, where the sponsors study is being conducted. Along with
other duties andresponsibilities of a CRA ,
there is a lot that the CRA has to do to conduct a clinical trial monitoring.
