Senior Strategic Medical Writer - Remote

📋 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
• Coordinates the review, approval, and quality control of other functions involved in the production
• Produces and maintains clinical and regulatory documents focusing on quality and compliance and
• Develops knowledge of US and international regulations, requirements, and guidelines pertaining to
• Participates in execution of tactical process improvements.

🎯 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 a comprehensive knowledge of medical and
• Proficient in assimilating and analyzing complex data.
• Experience writing and editing clinical and regulatory documents following guidelines and
• Understanding of drug development, clinical research, study designs, biostatistics, pharmacology

🎁 Benefits

• Comprehensive package of benefits including paid time off (vacation, holidays, sick)
• This job is eligible to participate in our short-term incentive programs.