Medical writer
Medical Writer
A Medical Writer (pronunciation: /ˈmɛdɪkəl ˈraɪtər/) is a professional who applies principles of Clinical Research and Regulatory Writing to produce well-structured, clear, and concise documents for the Healthcare Industry.
Etymology
The term "Medical Writer" is derived from the Latin words 'medicus' meaning 'physician' and 'scriptor' meaning 'writer'. It was first used in the late 20th century when the need for specialized writers in the medical field was recognized.
Role and Responsibilities
A Medical Writer is responsible for creating a variety of documents that include Clinical Trial Protocols, Patient Information Leaflets, Regulatory Submission Documents, and Medical Journal Articles. They ensure that these documents are compliant with Regulatory Guidelines and are written in a manner that can be understood by the intended audience, which may include healthcare professionals, patients, or regulatory authorities.
Skills and Qualifications
Medical Writers typically have a strong background in the life sciences, often holding advanced degrees in fields such as Biology, Pharmacy, or Medicine. They also possess excellent writing and editing skills, a keen attention to detail, and a thorough understanding of the Ethical Guidelines that govern medical writing.
Related Terms
- Clinical Research: The process of testing new treatments or medications in people to determine their safety and effectiveness.
- Regulatory Writing: The creation of documents that are submitted to regulatory agencies to seek approval for drugs, devices, and biologics.
- Healthcare Industry: The range of companies and non-profit organizations that provide medical services, manufacture medical equipment or drugs, provide medical insurance, or otherwise facilitate the provision of healthcare to patients.
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