Senior Strategic Medical Writer

📋 Description

• Prepares clinical and regulatory documents needed for the development of AbbVie drugs and/or
• Functions with a moderate degree of autonomy on draft materials, but relies on review by subject
• Develops knowledge and understanding of submission strategies.
• Coordinates the review, approval, and quality control of other functions involved in the production
• Arranges and conducts review meetings with the team.
• Produces and maintains clinical and regulatory documents focusing on quality and compliance and

🎯 Requirements

• A minimum of 4+ years of bio-pharmaceutical industry experience in global pharma, biotech, life
• Bachelor's Degree or higher required; scientific discipline preferred.
• Outstanding written and oral communication skills, with comprehensive knowledge of medical and
• Proficient in assimilating and analyzing complex data.
• 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) matching
• Short-term incentive programs