Associate Director, Global Regulatory Affairs, Central London, £60 000 - £80 000.

Our client is a well established pharmaceutical company situated in the heart of London and therefore surrounded by at least half a dozen mainline stations. If you enjoy the city life surroundings, this is an ideal location and company for you. In addition, with such a position, this post comes with many added perks. This company has a global presence. Working in the European Head Quarters, this is a position that will require occasional travel.

You will be involved in Product Development, so early stage experience is essential. Oncology experience is also essential.

You won’t have a team of people working underneath you. The responsibility will be solely on you or you may work with one other technical expert.

Working on global project teams. The oncology products that you are working on will be biological. So some biological experience would be preferred.

Provide regional regulatory therapeutic area strategic guidance on development projects and marketed products.

Additionally, develop highly functioning regional regulatory therapeutic area development team

Represent regional regulatory therapeutic product development team to regulatory upper management

Also, serve as regional therapeutic area regulatory representative for specific development projects or marketed products

Requirements

Very experienced in Oncology
Development experience is essential
Helpful to have management experience but not essential.
Centralised procedure.
Not necessary to have experience in all phases, just development.

To find out more information about this position, please contact Abid Kanji on 0207 940 2108 or email him on