Analyze The Field Of Clinical Research Associates (CRA)

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Clinical research associates (CRAs) coordinate the collection, distribution and storage of data obtained during clinical research trials, such as those which test drugs and medical products. In addition to ensuring that trials stay on track with clinical objectives and comply with federal regulations, they may analyze data, create reports, make presentations, monitor individual cases of testing participants, explain procedures to participants and family members and use reference material to conduct additional research. They also maintain databases of patient information, draft correspondence and gather data used in grant proposals and budgeting. Clinical research associates are employed by pharmaceutical companies, scientific research organizations, academic institutions and government agencies throughout the United States. Since the demand for newer, …show more content…

Clinical Research is a field that is expanding at an exponential rate due to the inception of new medical technology and increased demand on non-invasive medical procedures.

The evolution of clinical research traverses a long and fascinating journey. From the first recorded trial of a vegetarian diet in biblical times to the first randomized controlled of trial of streptomycin in 1946, the history of clinical trials covers a wide array of trials. 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. The CRA may work directly with the sponsor company of a clinical trial, as an independent freelancer or for a contract research organization (CRO). A CRA ensures compliance with the clinical protocol, checks, monitors, and maintains site activities, makes on-site visits, reviews case reports, and communicates with clinical research coordinators, and

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