Associate Director, Technical Writing

Responsibilities

• Lead planning and development of technical and scientific documents, including technical reports, protocols, summaries, presentations, and cross-functional deliverables
• Translate complex scientific data into clear, concise, and fit-for-purpose content for diverse audiences
• Ensure consistency, accuracy, and quality across documents, including alignment in messaging, structure, and terminology
• Partner closely with CMC, Nonclinical, Quality, and other functions to develop and refine written materials
• Establish and maintain templates, style guides, and best practices for technical writing and data presentation
• Drive continuous improvement in writing processes, tools, and standards
• Provide guidance and mentorship to internal contributors to elevate overall writing quality and effectiveness

Qualifications and Experience

• Bachelor’s degree in life sciences or a related discipline, with significant relevant experience; advanced degree (MS, PhD) preferred
• Extensive experience in technical or scientific writing within biotech or pharmaceutical development
• Strong ability to distill complex scientific information into clear, structured narratives
• Experience working across cross-functional teams and managing multiple deliverables
• Excellent writing, editing, and communication skills

Benefits

This role is based in our Lexington, MA office and requires employees to be onsite five days per week

Pay

$190,000 - $205,000 USD