Regulatory Affairs Consultant, Clinical, CTAs, International and EU, 30-50k+, North London, UK
Location:North London, England, UK
Salary: Above average and reflective of experience
Work as a regulatory consultant for a range of blue chip clients and clinical trials for one for the best developed companies in the Pharmaceutical industry. You can expect to be working inside world class facilities with access to the best training in the industry. You will be covering International and EU clinical trial applications (CTAs) as well as CTDs and trial protocol.
You will have the opportunity to work across a variety of clinical trials covering regulatory matters from a UK and International prospective. The work is both broad and varied meaning you are not going to get pigeon holed into one area.
Required Experience:
*18 months+ experience in Regulatory Affairs
*Industry Experience in a CRO or Pharma
*Strong knowledge of clinical documentation
Additional Experience:
*Oncology, CNS, Dermatology or Pain experience
*CTA submissions and creation
*Line Management/Project management experience
*Dealing with ECs and submissions
*Phase experience from phases I-IV
*CTD experience
*Experience in post marketing submissions and variations
Don't miss out on this chance to expand in your career! Contact Matt Beedle by calling 00442079402105 or email your current CV to m.beedle@nonstop-recruitment.com
