Senior Medical Writer - (Wilmington, DE)

This position is responsible for the development of clinical documents for worldwide submissions to regulatory authorities. Works directly with multidisciplinary project teammates with the goal of independently writing scientifically valid, complete, and consistent documents, such as clinical study reports (CSRs), investigator’s brochures (IBs), and select clinical Module two summary documents. The Senior Medical Writer may be responsible for the medical writing activities for 1 or more compounds and may contribute to major submissions. Understands the clinical research processes and global regulatory document standards. Demonstrates strong interpersonal and management expertise and can interpret and describe results. This position reports to the Head of Medical Writing.