Regulatory Submission Operations Specialist

Build our future together:

Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Regulatory Submission Operations, Specialist — IRAS/MHRA to join our Regulatory Submission Operations team in a hybrid role. In this role, you will be responsible for the end-to-end management of MHRA Clinical Trial Authorization (CTA) submissions via the IRAS portal — including portal form completion, document management, and RFI alert triaging — while working closely with Regulatory Affai...