Fantastic opportunity to join a top Pharma with some of the best-selling products in the business. Operating within the company's Established Products Group, you will function as a 'Regulatory Expert', overseeing Strategy throughout Western Europe. Regulatory Product Development experience is key with a particular focus on Phases II and III and planning for an MAA to be registered through Centralised Procedure.
This role will encompass Regulatory Strategy, Affiliate liaison and the maximisation of commercial possibilities of the company's products and development compounds within the geographical region. You will have a minimum of 8 year's experience in European Regulatory Affairs including full pipeline knowledge from CTA's through to MAA's and Post marketing. European Procedures working knowledge is required, particularly Centralised Procedure. You will possess good Commercial understanding of the business and be adept in project managing and multi-tasking.
Our client is prepared to offer a very attractive remuneration package for the right candidate including a competitive salary, cat allowance, bonus and excellent benefits including a final salary pension. An excellent working environment within a highly professional division awaits the appropriate individual.
If you are interested in this, or any other Regulatory Affairs opportunity, please call the Key People Regulatory Affairs team on 01727 811 634 or email on: regs@keypeople.co.uk