This is what you will do:

This position is accountable for the timely preparation of high quality, regulatory-compliant clinical document deliverables for Alexion. This position will support the medical writing (MW) activities for one or more clinical programs. This position will function with moderate supervision.

You will be responsible for:

• Supporting clinical project teams by authoring and managing the development and completion of high-quality clinical regulatory documents including, but not limited to, clinical study protocols and amendments, clinical study reports, Investigator's Brochures and updates, and clinical Common Technical Document components (eg, Module 2 summaries).
• Ensuring strategic organization, clarity, accuracy, format, and consistency of scientific content.
• Representing MW cross-functionally and with external vendors, negotiating timelines as necessary.
• P...