The Senior Medical Writer will research, create, and edit all documents associated with clinical research. Responsibilities also include: acting as primary client contact for medical writing projects, working with other PAREXEL departments and clients to set and meet internal/external deliverable timelines, project leadership, and training and support of junior medical writing staff.
• Demonstrated understanding of clinical research, the drug development process, and industry guidelines and regulations, e.g., ICH-GCP. • Extensive clinical/scientific writing skills. • Scientific background essential; writing experience includes multiple clinical documents: study reports, study protocols, or CTD documents or similar. • Fluent in written and spoken English with appropriate attention to phraseology, grammar, and punctuation.