Description
A global Pharmaceutical in the South East of England have an initial 6 month, rolling contract opening for a Regulatory Affairs Consultant on their EMAE team.The successful candidate will provide regulatory leadership and strategic direction for the R&D department, and interface with other functional members of assigned project teams; submit dossiers, variations and renewals via CP/DCP/MRP and National procedures; and liase with Regulatory agencies to facilitate the approval of submissions.
You will have exceptional hands on Regulatory Experience in a EU/Globally focused role, with a proven ability to consistently deliver to time, cost, and quality standards.
If this is of interest to you and you would like to find out more information on this position or any other regulatory affairs positions, please contact Colm Tobin on or please email c.tobin(a)realstaffing.com.