Medical Writer II

Responsible for creating high-quality, scientifically accurate medical and scientific documents. The role may involve tasks such as writing and editing study protocols, informed consent forms, clinical study reports, and other study-related documents. Additionally, the Medical Writer II may be responsible for reviewing and summarizing scientific literature, assisting with the development of study-related presentations and posters, and ensuring that documents comply with regulatory requirements and guidelines. Prepares protocols and CSRs, including interpretation of clinical data and statistical results as appropriate Work under guidance from colleagues to assist development of protocols, CSRs and other clinical documents on complex studies and programs Prepare and review patient safety narratives Leads project management and coordination of narrative projects Oversee and coordinate other writers on CSR appendices compilation. Good attention to detail, strong organizational skills, and the ability to work effectively in a team environment are also important.