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A clinical research associate (CRA), also called a clinical monitor or trial monitor, is a health-care professional who performs many activities related to medical research, particularly clinical trials. Clinical research associates work in various settings, such as pharmaceutical companies, medical research institutes and government agencies.
According to the RACC, the CRA designation carries numerous benefits to those who hold it, such as recognition among professionals, a sense of personal satisfaction, indication of expertise in the administration of sponsored research endeavors, greater opportunities for employment, greater opportunities for advancement, robust credibility, and the ability to serve as a role model to research ...
A Clinical Research Coordinator (CRC) is a person responsible for conducting clinical trials using good clinical practice [1] (GCP) under the auspices of a Principal Investigator (PI). Good clinical practices principles have been defined by Madelene Ottosen, RN, MSN, of The University of Texas Health Science Center at Houston [ 2 ] as:
A clinical research assistant or clinical research associate is employed by a hospital or medical research centre, who is involved in the administration of clinical trials. They may assist a senior investigator with recruiting and enrolling research subjects, as well as with correspondence and grant applications.
Clinical monitoring is the oversight and administrative efforts that monitor a participant's health and efficacy of the treatment during a clinical trial.Both independent and government-run grant-funding agencies, such as the National Institutes of Health (NIH) [1] and the World Health Organization (WHO), [2] require data and safety monitoring protocols for Phase I and II clinical trials ...
3 Job titles. 4 Laws. ... Clinical research associate or Clinical Research Assistant in clinical trial; Commander, Royal Artillery ... Corona Australis (CrA), ...
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