You will manage end-to-end regulatory submissions for investigational products, working with global regulatory teams, clinical operations, and technical experts. You will plan, prepare and submit clinical trial applications (CTAs) and related documents across multiple regions, ensuring timelines and regulatory requirements are met. We value clear communicators who are organised, collaborative and curious. This role offers growth, meaningful impact and the chance to help GSK unite science, technology and talent to get ahead of disease together.

This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: