Excellent opportunity at Associate Director level with a leading bio-pharmaceutical company. This is a fantastic opportunity for an experienced regulatory professional to work with a leading light in the pharmaceutical industry. Berks/Bucks/Middlesex location.
This is an extremely visible role reporting into the TA Head and would be responsible for European regulatory strategy within regulatory development for. Candidates will need strong experience from CTAs through to licence applications and post approval activities. Antiviral experience would be an advantage and candidates would need good experience with centralised procedures.
The client have a number of compounds in phases II-III of development with one MA coming up in the near future. Candidates will need strong experience with European regulatory strategy and strong experience liaising with global teams (US).
If you are interested in this, or any other Regulatory Affairs opportunity, please call Adam Griffin on + 44 1727 817 648 or email: agriffin@keypeople.co.uk
"regulatory" "regulatory affairs" "CTA" "MAA" "regulatory director" pharmaceutical" "biotechnology" "senior regulatory manager"