Senior Strategic Medical Writer - Remote

About this role

📋 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 We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick) This job is eligible to participate in our long-term incentive programs.

Source listing: empllo_remote