Position Overview: We are seeking an experienced Senior Medical Writer to produce clear, accurate, and compliant clinical and regulatory content. This role supports the development of documents essential to clinical research and regulatory submissions.
Responsibilities
- Write and edit protocols, clinical study reports, safety summaries, and other scientific documents
- Ensure all materials meet regulatory standards and internal quality benchmarks
- Collaborate with clinical, statistical, and regulatory professionals to gather and interpret data
- Revise documents based on team feedback and evolving project needs
- Maintain consistency across multiple documents and therapeutic areas
Qualifications
- Advanced degree in life sciences or related field
- Proven experience in medical writing within clinical research or pharmaceutical development
- Strong understanding of GCP, ICH guidelines, and regulatory requirements
- Excellent command of scientific language and attention to detail
- Ability to manage multiple projects and meet deadlines in a fast-paced environment
This role is ideal for a detail-oriented professional committed to scientific excellence and clear communication in a regulated environment.
