Senior Medical Writer/Principal Medical Writer

📋 Description

• Lead the 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
• Ensure smooth and effective document management from start to finish (from template to final
• Independently formulate key messages from clinical study data
• Author complex content using knowledge/skills and understanding of processes

🎯 Requirements

• BS degree or equivalent in a scientific or medical discipline with relevant writing expertise
• 5+ years of experience as a Sr. Medical Writer in the sponsor and/or CRO setting, or 7+ years of
• Proficiency with Microsoft Windows, Teams, Word, Excel, Adobe Acrobat, and PowerPoint
• Clear understanding of applicable regulations (e.g., 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 with