GlaxoSmithKline logo

Regulatory affairs

Charged with ensuring that our patients can be confident in the efficacy and safety of our products, the regulatory affairs team subjects all new drugs to the most rigorous standards testing.

This means that as well as collecting, collating and evaluating scientific data, you'll be keeping track of changing legislation and building strong relationships with other functions across the business, providing guidance and expertise wherever possible.

You'll also prepare documents for submission to obtain approvals for clinical trial, and make applications for marketing authorisation.

It's the kind of role that would be ideal if you're someone with a passion for science, plus a desire to develop your skills outside of the laboratory.



Back to top
Image of disability symbol
Accessibility and disability