Responsible for creating and revising documents related to IFP standards and supporting Quality partners. Collaborates cross-functionally, manages document workflows, and coaches document owners.

The Senior Medical Writer will author and review documents for clinical trials, ensuring compliance with regulatory requirements. Responsibilities include preparing protocols, reports, and submissions while collaborating with diverse project teams. The role emphasizes clear communication and knowledge sharing to enhance processes within medical writing.

The Technical Writer III coordinates and creates cGMP manufacturing documents while ensuring accuracy and adherence to regulatory procedures. Responsibilities also include responding to feedback and supporting technical writing activities.