A Clinical Research Associate (CRA) can be employed directly by the sponsor companies (such as Pharmaceutical, Biotechnology, or any research company) of clinical trials or by Contract Research Organizations (CROs), also referred to as Clinical Research Organizations. According to ICH GCP, these organizations conduct clinical trials on behalf of the sponsor companies. Let’s learn about the types of clinical trial site visits conducted by CRAs. The primary responsibility of a CRA is to ensure that the rights, safety, and well-being of subjects participating in clinical trials are protected. The CRA acts as the main mode of communication between sponsors and the site. A Clinical Research Associate qualifies, initiates, monitors, and closes the clinical trial sites assigned to him/her. Based on their level of experience, CRAs can be hired at various levels such as CRA Level I, II, III, and as Senior CRA by employers. Some common on-job responsibilities of CRAs include: Required skills for a Clinical Research Associate include: The process of outsourcing and flow in clinical trials involves: I am listing the types of Clinical Trial Site Visits conducted by CRAs, which may vary depending on industry practices: In conclusion, these are the basic types of Clinical Trial Site Visits conducted by CRAs. I will provide detailed information about each visit in upcoming articles. Article By: Shahenaz Karadesai