B Sc Clinical Research

As part of studying Clinical Research and Healthcare Management one learns how to investigate new medical products and devise methods to ascertain their efficacy and safety. It involves designing treatment plans and regimes for better health, relief or reduction from symptoms of a disease, treatment diagnosis, etc.

The later part of this article will acquaint you with B.Sc. Clinical Research and Healthcare Management course details covering information on the eligibility for sitting in this exam, course syllabus, and scope for the kind of jobs you can get once you finish this course. You will also learn what to expect for a Clinical Researcher’s salary in India.

Entry Level Eligibility

 
The selection process is quite detailed with a written exam conducted by ICRI which is followed by group discussion and a personal interview.

Clinical research is a vast area and specializing in any one of the below-mentioned areas would give a better B.Sc. Clinical Research and Healthcare Management Salary in India:
● Clinical Data management – This role involves collecting data from any tests, treatment, or trials that are performed. They specialize in figuring patterns in clinical data to support government approval for a drug of product.
● Medical writing – These specialists develop foundational capabilities to write and communicate about health. They are well versed in writing scientific documents of various types. These writings include regulatory and research-related documents. Other kinds of writing that come under this specialization are drug-related educational and promotional literature, journal manuscripts and abstracts, articles for healthcare websites or health-related magazines, and many more.
● Product safety specialist – A product safety specialist falls under regulatory affairs. They are occupational health and safety specialists who identify hazards in the workplace. Their job is to investigate workplaces to ensure proper standards of safety, health, and environment are maintained. They collect samples of materials that could be potentially toxic to evaluate them. They also conduct training on many topics like emergency preparedness, etc.
● Clinical Trial Auditor – They conduct and evaluate the trial conduct to make sure the trial adhered to protocols, SOPs, GCP, and other regulatory requirements that apply.
● Clinical Research coordinator – This is a specialized research coordinator profile that supports and facilitates the daily clinical trial activities. They coordinate and work with various departments like PI (Principle investigator), sponsor, and institution while providing guidance on financial, personnel, and other clinical study aspects.
● Drug development – This specialization helps in developing new drugs for the public.