AddressMedical writers are required within a range of different settings such as within CROs, pharmaceutical companies and medical communications agencies, therefore exact responsibilities will vary.
As a general rule, they write a range of clinical documents from initiation to completion, producing high-quality, clear and accurate work. They may also be required to contribute to document quality control (reviewing data accuracy, formatting and appropriateness of language, and compliance to industry guidelines) as well as evaluate the data to be included within documentation. They can be involved in writing:
- Clinical trial protocols and publications
- Study reports
- White papers
- Consumer drug/medical device information
- Magazine and newspaper articles
- Medical and healthcare advertisements
- Insurance policy documents
- Medical books
- Advice leaflets and websites
- Press releases
Skills: Technical Writing, study reports , Quality Control, Publications, white papers, Protocols
Experience: 0.00-2.00 Years
