As a Clinical Research Associate (CRA), it is important during all site visits you are self-confident, knowledgeable and a trustworthy partner for all stakeholders throughout all stages of a trial. A CRA is involved in all stages of a clinical trial, including identifying and setting up an investigational site, monitoring of the trial and then closing it down. The CRA will also act as the main line of communication between Sponsor and Investigator and is the primary contact for the site. In this course, student will gain insight into basic monitoring tasks, how to communicate and present a trial to site staff and act with confidence in a CRA position.