A clinical research associate (CRA) works both at clinical sites and sponsor locations. They are health-care professionals who perform many activities related to medical research, particularly clinical traits. CRAs are also called a clinical monitor or trial monitor. During a trial, the CRA conducts regular site visits (virtually and physically) to ensure proper progress and record keeping on the part of the clinical site. CRAs are often responsible for multiple trials at one time, which can mean significant amounts of travel between these sites. In some cases, a CRA may be assigned to a specific geographical region, which can limit travel. Typically, a clinical research associate does not have direct contact with the participants involved with the study. However, CRAs must be able to work in a collaborative environment coming into frequent contact with the clinical team at the study site and the supervisors from the study sponsor. In short, a CRA is focused more on data, accuracy, and quality control.

Multiple Contributors

4K resources

0

0

0

Like