Associate Director, Technical Writing
Kiniksa Pharmaceuticals
June 27, 2026
On-site
Lexington, MA
Corporate Functions
Associate Director, Technical Writing
Responsibilities:
- Lead planning and development of technical and scientific documents (technical reports, protocols, summaries, presentations, and cross-functional deliverables)
- Translate complex scientific data into clear, concise, fit-for-purpose content for diverse audiences
- Ensure consistency, accuracy, and quality across documents (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
Standout Skills for Impact:
- Experience supporting early- to mid-stage development programs
- Familiarity with CMC and nonclinical content
- Ability to implement writing standards and improve documentation practices
Qualifications and Experience:
- Bachelor’s degree in life sciences or related discipline with significant relevant experience; 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
Work Location:
- Onsite in Lexington, MA; requires onsite five days per week
Pay Range:
- $190,000 - $205,000 USD
Responsibilities:
- Lead planning and development of technical and scientific documents (technical reports, protocols, summaries, presentations, and cross-functional deliverables)
- Translate complex scientific data into clear, concise, fit-for-purpose content for diverse audiences
- Ensure consistency, accuracy, and quality across documents (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
Standout Skills for Impact:
- Experience supporting early- to mid-stage development programs
- Familiarity with CMC and nonclinical content
- Ability to implement writing standards and improve documentation practices
Qualifications and Experience:
- Bachelor’s degree in life sciences or related discipline with significant relevant experience; 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
Work Location:
- Onsite in Lexington, MA; requires onsite five days per week
Pay Range:
- $190,000 - $205,000 USD