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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.
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.
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).
In academic and research institutions, as well as in some industries, a research associate is a common professional position. Typically, research associates work with other researchers, scientists, and faculty members on a variety of research projects. The duties of research associates can change depending on the organization and the particular ...
Role of the clinical data manager in a clinical trial Job profile acceptable in CDM: clinical researcher, clinical research associate, clinical research coordinator etc. The clinical data manager plays a key role in the setup and conduct of a clinical trial. The data collected during a clinical trial form the basis of subsequent safety and efficacy analysis which in turn drive decision making ...
Statins are linked to better health outcomes in older adults over the age of 70 with or without previous cardiovascular disease, a new study finds.
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