The Principal Medical Writer is responsible for leading and writing clinical and regulatory documents for drug and/or device development in support of company objectives.

Responsibilities

• Independently prepares most clinical and regulatory documents needed for the development of AbbVIe drugs and/or devices.
• Coordinates the review, approval, and quality control of other functions involved in the production of clinical and regulatory documents. 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.
• Contributes to project management strategies and develops ability to lead team members, driving submission objectives.
• Recommends, leads and/or participates in implementation/execution of tactical process improvements.
• Develops expert knowledge of US and international regulations, requirements, and guidance associated with preparation of regulatory documentation.
• Identifies and proposes solutions to resolve issues and questions arising during the writing process, including resolution or escalation as appropriate.
• Learns and applies therapeutic area and product knowledge to scientific projects and business improvement projects.
• Works independently with R&D Quality Assurance to address inquiries and draft responses, maintaining an inspection-ready approach.