Clinical research associate training program :- Clinical research associate (CRA) are trained clinical research professionals who takes an active role in clinical trials to assess prospective drug candidates for their effectiveness and to ascertain that they are safe for human use. They do trials on novel as well as on medications available in the market for human consumption and are employed by either a contract research organization which works on behalf of pharmaceutical company or a pharmaceutical company directly.
A superior clinical research associate training program includes study modules that teach, how to select a study site, initiate a study, study set-up and closing the clinical trial at site, how to create essential manuscripts, global regulatory requirements, ethics and ethics committees, guidelines pertaining to ICH-GCP in clinical trial conduct, different clinical research stake holders and their responsibilities, timely reporting of adverse events and topics relating of regulatory documentation, good clinical data management and medical writing. The aspects of Principal investigator (PI) selection, site monitoring and Informed Consent Form (ICF) & Case Report Form (CRF) filling procedures must be lucidly explained with their importance in clinical research.
The clinical research associate training institute of your choice for training should have credentials with respect to clinical research professionals and total number of years of institutes’ existence will help evaluate the service provider.
James Lind Institute is helping the student community since earlier times in clinical research domain. Our inimitability lies in the eminence and mode of training. To know more about JLI please browse through our website at www.jli.edu.in.