Regulatory Documentation Scientist - Top Pharma Company

Do you have a keen eye for report writing? Enjoy the detail and accuracy? How about doing this for one of the top pharmaceutical companies in the UK?

I am currently working with one of the top pharmaceutical companies in the UK who are looking to increase their Regulatory Documentation team by adding a new report scientist to their ranks. This is a long term contract position lasting 12 months with potential for extension. Keeping you fully stable for a year! No more juggling clients and contracts just one FTC to see you into the new year.

The role will consist mainly around the writing and submissions of RMP's, Benefit Risk Evaluations, DSUR's and ensuring quality and the development of these documents up to submission. If you already have previous experience with either PV documents or Regulatory documents you will be very well versed in what these will entail.

Working with this pharmaceutical company ensures that you work with some of the most innovative and broad pipelines in the Industry, keeping your documents interesting and having continual updates and changes from project to project, because who wants to do the same product over and over again?

Based in Welwyn Garden city ensures you are far enough away from London that you don't have to deal with London rent and house prices while still enjoying the transport links to get you to Central London easily!

The minimum requirements for this role are as follows:

BSc in Life Sciences
Previous Experience in Regulatory/Pharmacovigilance report writing

If you are interested then send your most updated CV to G.Collins@nonstop-recruitment.com alternatively call me; Greg Collins on 0207 940 2105 and we can discuss the opportunity, but be quick great chances in this company don't last forever!