Regulatory Affairs Jobs

Within Regulatory recruitment we recruit for a range of positions from Regulatory Affairs Executives/Associates through the Global Head positions available on a permanent, contract or freelance basis.

Experience in either clinical regulatory activities or in post-marketing activities is valuable for our prestigious clients. Clinical regulatory affairs include compiling and preparing Clinical Trial Applications (CTA's) and Marketing Authorisation Applications (MAA’s), post-marketing activities include maintenance and managing the drug product’s lifecycle.

Our candidates are well-educated in scientific or related disciplines and have previously held positions at national regulatory bodies or respective regulatory authorities, and have specialist experience in a variety of regulatory environments, providing them with a good understanding of all aspects of the clinical product lifecycle.