Principal Strategic Medical Writer

📋 Description

• Independently prepares most clinical and regulatory documents needed for the development of AbbVie
• Coordinates the review, approval, and quality control of other functions involved in the production
• Arranges and conducts review meetings with the team.
• Works closely with the team(s) on document authoring and content strategies.
• Communicates deliverables needed, writing process, and timelines to team members.
• Holds team members accountable to agreed-upon project dates.

🎯 Requirements

• A minimum of 5+ years of bio-pharmaceutical industry experience in a global pharma, biotech, life
• Bachelor's Degree or higher required; scientific discipline preferred.
• Outstanding written and oral communication skills, with a comprehensive knowledge of medical and
• Proficient in assimilating and analyzing complex data.
• Extensive experience writing and editing clinical and regulatory documents following guidelines and
• Familiarity with industry standards like CONSORT and PRISMA guidelines.

🎁 Benefits

• Paid time off (vacation, holidays, sick)
• Medical/dental/vision insurance
• 401(k)
• Eligible to participate in long-term incentive programs