Senior Medical Writer/Principal Medical Writer

📋 Description

• Leading development of high-quality and on-time clinical study documents
• Clinical document planning, writing, editing/formatting, and performing QC review
• Develop documents in compliance with Precision MW Style Guide, Precision SOPs, applicable
• Planning, writing, editing, formatting, and QC review of clinical documents including protocols
• Ensuring smooth and effective document management from template to final approved version
• Independently formulating key messages from clinical study data

🎯 Requirements

• BS degree or equivalent in a scientific or medical discipline with relevant writing expertise
• 5+ years of experience as Sr. Medical Writer in sponsor/CRO setting OR 7+ years as Principal
• Proficiency with Microsoft Windows, Teams, Word, Excel, Adobe Acrobat, and PowerPoint
• Clear understanding of applicable regulations (ICH, FDA, GCP), clinical trial transparency
• Impeccable attention to detail and ability to complete writing assignments in a timely manner
• Ability to work effectively in a fast-paced environment with multiple high-priority projects