|Combine your scientific knowledge with quality writing skills to ensure the documents you prepare are clear and easy to understand.|
This course covers the general principles of writing documents for clinical research in the pharmaceutical industry. It provides advice and ideas on what your target audience is looking for so that your message comes across as you intended. The importance of clear and concise writing is emphasised, with hints and tips on how to keep your reader’s attention on what you have written. How to communicate key messages will be discussed and how this varies between different documents such as protocols, reports or patient information sheets. In the final session, we will llok at how to review a document, and how to provide constructive feedback to the document author. The importance and principles of Quality Control checking are covered briefly.
By the end of this course, you will be able to:
- combine your scientific knowledge with quality writing skills to ensure that the documents you prepare are clear and easy to understand
- write the right document for the right audience
- include the right information
- select the structure and style that is most effective for your audience