SENIOR REGULATORY AFFAIRS ASSOCIATE - CUTTING EDGE SPECIALIST BIOPHARMA!! - CAMBRIDGE!!
REGULATORY DEVELOPMENT FOCUS - PHASES I AND IV THROUGH TO POST MARKETING AND COMMERCIALISATION, HIV PORTFOLIO
Clinical /Development Regulatory background with Registration and Post marketing an ideal combination.
Our client is a top Specialist Pharma Company with an excellent working environment. You will be concentrating on Clinical/Development Regulatory: CTA''s, IMPD''s, Protocols, Clinical Regulatory amendments & variations. National Submissions/MRP, DCP and CP; Post marketing: Variations, Renewals; Labelling, PIL''s SmPC''s. This organisation has a superb pipeline of products across a number of Therapeutic areas. Project management.
An excellent salary, bonus and benefits are on offer for the successful candidate.
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 j.turner@NonStop-pharma.com