The world of drug development is vast and can be overlycomplicated for the uninitiated. However, modern uses of technology and the supply methods for that technology mean that uses of clinical trial academics tools and models are accessible to those who need them. Academic licences for gene-editing equipment, in vivo models, and more, are all easier to access and have less monetary and production-time pressure to allow students to learn and test, stress-free. Here are 4 things to be aware of as someone looking into clinical trials for academic purposes.
Bursaries and Expenses
Education is often an expensive journey, but specialized equipment and areas of expertise often have specific payment systems in place. For example, the Institute of Clinical Trial academics offers a bursary of over $7000, and other large research bodies, like Cancer Research, offer Research Bursaries as a short-term relief for academics to break into a project.
Your place of education may have specific expense forms available for your research, and if not, should be able to help you find a project that in turn is funded itself, taking the strain off the individual academic.
Follow the Leader
Technology has been advancing exponentially in almost every aspect of science – computing, medicine, psychology, and food growth, just to name a few. By keeping a close eye on industry leaders and key technologies, you can associate yourself with the areas that are receiving the best models and funding. For example, following a project that utilizes PiggyBac, the best gene delivery and editing system in the industry right now (who also have an academics licence), will guarantee that when you do get onto a project, it’s one at the forefront of at least one area of the craft.
Drug creation and clinical trials are pivoted on collaboration. Between managers, stakeholders, suppliers, and researchers, a lot of people go into making one product. Being a Clinical Trial academics and knowing a lot of clinicians is fine, but it’s variety and keen interest that sets people apart. Finding like-minded but differently-skilled individuals to add to your contact list is a great way to expose yourself to the variety of the industry and find out more about how each level operates. In time, this will make you more easily able to slip into a project and understand, on a personal level, everyone’s role.
Learn Your Acronyms
It’s no secret that regulatory bodies as well as Clinical Trial academics suppliers and companies are multi-faceted and complicated. The Case Western Reserve University, for example, operate its cancer research under the Protocol Review and Monitoring Committee (PRMC), like many others. This is an important acronym to know if cancer research is your field. Add in the FDA (Food and Drug Administration) and its specific subsets like the CBER (Center for Biologics Evaluation and Research), as well as government branches, like the Health Insurance Portability and Accountability Act (HIPAA), and suddenly there’s an awful lot of conditions to fulfil and uphold to legally research drugs. Find an explanation of the acronyms and their bodies here, in the very first paragraphs before “Getting Started”.