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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 ...
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:
Research associates are researchers (scholars and professionals) that usually have an advanced degree beyond a Bachelor's degree such as a master's degree or a PhD.. In some universities/research institutes, such as Harvard/Harvard Medical School/Harvard School of Public Health, [1] the candidate holds the degree of Ph.D. or possess training equivalent to that required for the Ph.D.
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.
Entry-level jobs with this qualification are often clinical research-related. At the entry level, PMST specialists often place into clinical research associate, clinical research analyst, pharmacodynamic data observer, clinical research project manager, drugs and pharmaceutical control manager in clinical research project, etc.
Clinical data management (CDM) is a critical process in clinical research, which leads to generation of high-quality, reliable, and statistically sound data from clinical trials. [1] Clinical data management ensures collection, integration and availability of data at appropriate quality and cost.
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