Responsibility of a Research Assistant
When a trial has finished, the data collected is examined and interpreted by clinical research affiliates. The research affiliates spend plenty of time on the computer working with spreadsheets to analyze the results. Once the results are prepared, the research assistant shares the outcomes with associates of the analysis team and they evaluate the reports for presentation.
Next, the head specialist offers these reports to governing bodies, companies and organizations that will then choose whether the drug or piece of medical device becomes accepted for use in medical centers or by the public.
Other duties include contacting and testing study participants, getting in touch with and connecting with other people of the research group, performing literature searches, and obtaining and filing numerous consent and authorization documents and a variety of other management tasks.
Tip: As a research assistant; make sure that you are part of a legitimate and ethically approved Clinical Research Organization.
FDA (Food and Drug Administration) or MHRA (Medicines and Healthcare products Regulatory Agency) or are responsible for the regulation of all medicines and medical devices within their respective countries. If you are studying or plan to become a research assistant, make sure to to look at companies that have licenses for medicines that are granted only when a product meets high standards of safety and quality and serves for the purpose intended.
Without regulations and ethics, clinical research can be dangerous, with the right experience, monitoring and authoritative procedures in place, clinical research is a stepping stone to the evolution of healthcare and new medicines which is a benefit to human health as a whole.