How to start a career in clinical research training and the uses of clinical research training.

Only two decades have passed since clinical trials were conducted in India. In the early 1990s, large multinational pharmaceutical companies began conducting human trials through their offices in India. Multinational companies have benefited from their extensive experience in clinical studies acquired in the West to carry out successful trials in India following all international guidelines and regulations. Although successful, these companies faced many challenges in achieving measurable results and complying with the regulations governing clinical trials. One of the main challenges was the lack of awareness and training of clinical researchers and their staff. Many doctors were not uncomfortable with the idea of making their patients do not part of a clinical trial, nor did they have a good understanding of the drug development process. Only a few doctors who received good patient flows and a good reputation in the West participated in Indian clinical trials. Soon, companies began to realize the enormous potential of India as a region where new medicines could be developed faster and cheaper. This has led pharmaceutical companies to conduct more trials in the country with more trained doctors next to them. Although the challenges were many when clinical trials began in the country, most of them were collectively overcome by the industry. As the industry grows, many new challenges have emerged, such as those posed by India's changing regulatory environment and some old challenges, such as the need for formal training in clinical research, remain.

The need for clinical research training was emphasized by all teachers participating in clinical trials, such as study coordinators, principal investigators, clinical research partners, data managers, project managers, etc. In accordance with the ICH-GCP guidelines, all staff must be adequately trained in the study behavior. They should know the guidelines and regulations applicable to them that should be followed and should be familiar with their specific study documents, such as the study protocol.

To achieve this clinical research training, it is always recommended to enroll in a clinical training program at a known institute. You don't have to spend all your time attending classes. You can easily enroll in an online clinical research program such as the one offered by the James Lind Institute and reach the required and expected level of competence of a research specialist. A good online training program is enough to start working on the research industry.

The author of this article is a student at the James Lind Institute. With more than 5 years of experience, she is familiar with the problems students face in clinical research training.

Clinical research is a department of medical science that guarantees the safety and efficacy of medications, equipment, diagnostic products, and treatment systems for people. These can be used for protection, treatment, medical diagnosis or to reduce the symptoms of the disease. Clinical research training is unique to clinical practice.

Training to be a clinical research assistant involves the development of a purpose, methodology, and protocols for experiments to design case records used for data collection, communication, negotiation with regulatory authorities, communication with doctors and scientists for experiments, monitoring, and data verification at all stages. And correspondence.  Find an institute that includes practical training in your training program and offers professional assistance programs to gain value for your money.