SENIOR MANAGER/ASSOCIATE DIRECTOR, PROJECTS – INTERNATIONAL REGULATORY TEAM LEADER.

PHARMA AND BIOPHARMA PRODUCTS.

Working for a ‘blue-chip’ Pharma either in Hertfordshire or Switzerland you will have a minimum of 5 years International Regulatory Affairs experience across the Life-cycle from CTA’s and other Clinical Regulatory activity through to Registrations and Post marketing. and significant Product Development. In a European context you will have working knowledge of Centralised Procedure and ideally operated with a ROW team.

This could be your only opportunity to work for the industry’s premier organisation!!!

For a confidential discussion and to find out more information about this Regulatory role or any other Regulatory Affairs roles please contact our Senior Regulatory Manager Julian Turner on the Regulatory Affairs Team on 0207 234 0550 or by e-mail to Regulatory@NonStop-pharma.com