Principal Strategic Medical Writer - Remote

Overview

As a Principal Strategic Medical Writer at AbbVie, you will be responsible for leading and writing clinical and regulatory documents that support the development and communication of innovative therapies.

In Short

• Independently write clinical and regulatory documents.
• Coordinate review, approval, and quality control processes.
• Communicate deliverables and timelines to team members.
• Contribute to project management strategies.
• Develop expert knowledge of regulations for regulatory documentation.
• Identify and propose solutions to issues during the writing process.
• Apply therapeutic area knowledge to projects.
• Work independently with R&D Quality Assurance.

Requirements

• Bachelor's Degree or higher in a scientific discipline.
• Minimum of 5+ years of experience in the biopharmaceutical industry.
• Outstanding written and oral communication skills.
• Experience with clinical document writing and editing.
• Familiarity with ICH guidelines and regulatory requirements.
• Proficient in analyzing complex data.
• Ability to oversee multiple projects simultaneously.

Benefits

• Comprehensive benefits package including medical, dental, and vision insurance.
• Paid time off including vacation and sick leave.
• 401(k) plan for eligible employees.
• Participation in short-term and long-term incentive programs.