- Research, write, and edit clinical documents, including clinical study protocols, clinical study reports, IB, ICF, RMP, clinical plan outlines, and scientific manuscripts.
- Review statistical analysis plans and mock statistical output to assist in determining appropriateness of content/format for clinical writing.
- Provide medical editing review of draft and final documents.
- Perform literature searching and reviews as necessary.
- Medical related degree & 2Y+ medical writing experience.
- Experience in clinical study design and protocol development and CSR/writing.
- Fluent in English, both verbal and written.