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.