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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.
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.
Clinical Professor, Professor of Practice (usually non-tenure-track positions which can be full-time and permanent, but whose teaching tends to focus on practical rather than scholarly expertise; sometimes these categories have their own respective ranking hierarchies) Research Associate, Research Professor.
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 monitors execute the monitoring plan laid out by the sponsors and investigators of a clinical trial. Monitors may be referred to by many different titles, such as: Clinical Research Associate, "on-site" monitor, Clinical Research Monitor, Study Site Monitor and Quality Specialist. The number of clinical monitors depends on the scale ...
Clinical research is different from clinical practice: in clinical practice, established treatments are used to improve the condition of a person, while in clinical research, evidence is collected under rigorous study conditions on groups of people to determine the efficacy and safety of a treatment.
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:
An advanced professional degree provides further training in a specialized area of the profession. A first professional degree is an academic degree designed to prepare the holder for a particular career or profession, fields in which scholarly research and academic activity are not the profession, but rather the practice of the profession.
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