Senior Medical Writer, Regulatory Submissions

GlaxoSmithKline in Stevenage is seeking an experienced professional with advanced medical writing expertise to independently manage complex regulatory writing projects. The role involves authoring clinical regulatory documents and ensuring compliance with GSK standards and regulatory requirements.

The ideal candidate will possess a PhD and significant experience in clinical regulatory medical writing, demonstrating the ability to lead submissions and interpret complex data.

This position offers a hybrid working model, competitive salary, annual bonus, and comprehensive benefits.