Provides medical writing resource to the International Regulatory Group with respect to regulatory report, summary, and response writing. Prepares regulatory documents such as clinical study reports, Investigator Brochures and Annual Updates in-line with regulatory requirements and Gilead internal document standards. Medical writing activities at the level of single study reports and noncritical documents are performed without appreciable supervision. Additionally, is involved in the preparation of more complex regulatory documents with direction from Associate Director / Director level.