Excellent Regulatory Project Manager position focusing on development within a bio-pharmaceutical company. Unique opportunity to work for a top Director in Regulatory Affairs. Berks/Bucks/Middlesex location. Leading benefits.
This Biopharma rarely recruits in the area of Regulatory Development, so if you are interested, do not delay this application. This position is focused on Regulatory Development, so 4+ years experience in Phases I to IV is required.
This client is commercially very successful with a significant number of Clinical Trials in progress in numerous Therapeutic areas. The working environment is very dynamic, and with very much an EU focus there will be liaison with European Affiliates in addition to the USA. The candidate's background will need to include Clinical Trial Applications through to End of trail Notifications and MAA's. European procedure experience is required, preferably including Centralised Procedure but MRP or DCP experience may be considered if the candidate's Development experience is sufficiently strong. The ideal candidate will be working for an Ethical Pharma or Biotech company.
A competitive salary package is on offer.
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