A Clinical Research Associate (CRA), sometimes called a monitor, is responsible for overseeing clinical trials conducted at various research sites. A CRA serves as a liaison between the study’s sponsor and the research teams working onsite where the study takes place. CRAs play a critical role in the success and integrity of a trial and must be highly-trained in good clinical practice (GCP) guidelines. Many professionals want to become CRAs and the best way to achieve this is to gain the training, qualifications, and experience required to oversee clinical trials at multiple sites. Clinical Research Fastrack provides the high-quality training and experience that entry-level Clinical Research professionals need to jump into their roles and be successful. With this comprehensive training, our graduates are moving into a wide variety of Clinical Research positions, including CRA roles.