A trial is a branch of clinical research, which is a major component of medical research and it involves everyone including you. It consists of volunteers, doctors, and clinical researchers working together to learn more about diseases and how to improve health care for people. It includes the following branches;
Behavioral: This branch improves the understanding of human behavior and how it relates to diseases and health.
Health Services: This branch focuses on the way people access health care services and service providers, how much health care costs, and the results of the care to the patients.
Epidemiology: This branch focuses on improving the understanding of a disease by studying, the cause, patterns, symptoms, effects, prevention, and cures in specific groups.
Clinical Trials: This branch helps evaluate the effects of an intervention on health outcomes.
You're wondering why you should be a part of the professionals that engage in clinical trials, right? Let's give you some insider scoop. Clinical trials are at the heart of all medical advancement around the world, and it has one of the highest pay in all the medical field, ranging from $65,854 - $160,654 earnings as an annual salary. They look at new ways to detect, prevent, and treat diseases. They make sure to study new medical devices, new drugs, a new combination of drugs, new surgical procedures, new ways to use existing treatments, new ways of behavioral changes to improve health, new ways to improve the quality of life.
The main goal of all clinical trials done by clinical research professionals is to determine if the detection, treatment, prevention, experimentation, and behavioral approaches to health care are effective and safe. Clinical trials offer hope for people with illness, diseases, or healthy volunteers receive new treatments and care as well as take part in finding new ways to help others.
The clinical trial research process starts often in the lab, where the testing if new procedures or treatments in the laboratory on animals. The most promising of all treatments are now moved into clinical trials to experiment on human volunteers. The new treatments move through phases and all data are collected about the treatments, procedures, risks, and effectiveness of the new treatment or drug.
An institutional review board is set up to approve and monitor most of the clinical trials to ensure that they are risk-free or the risk reduced and that they have more benefits than harm to the health care department. They are responsible for reviewing clinical researches in order to protect the right and safety of people who take part in research, before, during, and after.
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