One of the finest Medical Writing Institute that provides training in Medical Writing is James Lind Institute (JLI). If are looking for online medical writing training programs that can be completed from any location by harnessing the power of internet, James Lind Institutes online medical writing programs are your best bet. JLI’s medical writing training covers training related to basic writing skills, pharmaceutical regulatory writing, medico marketing writing, academic writing and other important areas necessary for a medical writer. You have the option to choose between an Advanced Training Program that covers both Clinical Research & Medical Writing, and a standalone medical writing program which is the Professional Diploma in Medical Writing.
Clinical Trial Project Management is one of the most important functions within a Clinical Operations team. It is equally important for both Pharma-biotech companies conducting their own clinical trials as well as Contract Research Organizations that conduct clinical trials for sponsor companies. Good Project Management results in savings of costs and resources and leads to a high quality end product. Good Project Management results in a clinical trial being conducted smoothly and efficiently without any major problems along the way. It is said that Good Project Management is only as good as the Project Manager. So, it is important to have an experienced Project Manager running the project who knows all the tricks of the trade.
It is essential for you as a medical writer to learn and polish your proofreading and editing skills, even though a senior writer or an editor is available and will edit and proofread your work before it is submitted to the client.
A systematic approach for editing and proofreading:
– Helps you to find and correct unnoticed language errors.
– Gives you a chance to recheck, rearrange and polish your work.
– Helps you to enhance readability of your writing.
– Reflects professionalism by ensuring accurate and consistent work.
Writing educational reading material for patients and public at large can be an interesting break from the technical and scientific writing, written specifically for an audience with varied medical backgrounds. So what makes writing patient education brochures interesting? Well, a couple of things:
Different Source Content
Writing a patient education brochure is very different from technical writing. It involves searching information from all possible channels and resources, unlike technical writing where most of the content comes from lectures, presentations, scientific articles, research papers and event highlight bulletins.
The client might provide the basic information and material, but assembling the information in the brochure requires a good internet search for latest facts and data relevant to the topic. Journals and magazines available in the company library may also prove helpful.
In the earlier post we discussed that medical writers may be involved in creating post-event CD-ROM’s. Let us look at some simple steps that you should follow when working with CD-ROM’s:
A good post-event CD-ROM contains the following, so try to incorporate most of these in your CD:
• Introduction of the product or company, title of the event, & introduction of the speakers; preferably all in a simple and professional animated format.
• A complete footage of speakers with the presentation slides and audio in sync.
• Footage on the Q & A session, which may be clipped to relevant small individual clips.
• Some extra material such as slide presentations presented during the event, product information in PDF format, event pictures, CV’s of the speakers etc.
The increasing use of technologies such as multimedia devices and the internet has opened up new opportunities for the pharmaceutical and communications companies to achieve multiple objectives such as product marketing, creating company training programs, communicating with potential and existing consumers, conducting CME (continuing medical education) programs for physicians etc.
Some electronic projects (non-print publications) that may require a medical writers contribution in content development are:
Different types of editorial and non-editorial services are offered by medical and healthcare communications companies to their clients. Most of these clients are involved with the marketing of their products such as medicines, medical devices, health supplements, growth formulas etc.
All materials are developed as per the client requirements, and are mainly used as promotional tools for marketing campaigns of new medicines; devices etc, or simply to make the general public aware of a drug already available in the market. As obvious, these materials are prepared for a number of audiences such as the medical or healthcare professionals, patients or the general public.
Medical writers are an integral part of the pharmaceutical industry. Successful medical writers possess various key competencies such as flawless English language skills, flair for writing, ability to present medical data accurately, audience identification, commitment to quality, team skills, ability to meet deadlines etc.
Pharmaceutical industry, Contract Research Organisations (CRO’s) and communications agencies frequently hire medical writers in full time positions. They can also work as freelance medical writers and medical journalists. The nature of work of a medical writer varies from company to company. Those working with CRO’s and pharmaceutical companies are mainly involved with regulatory document preparation, while those who work with communication agencies are involved in preparing promotional and marketing related documents. Medical writers are involved in preparation of scientific documentation at all levels of drug development, and for this pharmaceutical companies have separate and well organized medical writing departments. Medical writers are also involved in consultancy services, for providing information on document templates, regulatory requirements, protocol information, branding & styling for the product, quality control, and presentation & marketing of the product. Medical writers in senior positions are often involved in handling additional responsibilities such as providing input in drug development programmes, trial designs, data analysis, product launch and marketing strategies.