Job Summary
A company is looking for a Senior Medical Writer responsible for creating high-quality documents to support research programs.
Key Responsibilities
- Serve as the Medical Writing representative on project teams and develop clinical protocols
- Create clinical study reports and safety narratives, ensuring compliance with regulations and client expectations
- Perform quality control and editorial review of documents, coordinating internal reviews and managing feedback
Required Qualifications
- Master's Degree in health-related sciences or a relevant field; advanced degree preferred
- Understanding of clinical research, drug development processes, and applicable regulatory guidelines
- Strong computer skills, particularly in Microsoft Word, Excel, and PowerPoint
- Ability to work well with a multi-disciplinary team of professionals
- Fluency in English is essential for communication and documentation purposes
Comments