Ra Consultant - Clinical Writing - Europe Wide

  • United Kingdom
  • Nonstop Consulting Limited

Our client, a multinational Clinical Research Organisation , is currently looking to hire a Regulatory Affairs Consultant to join their Regulatory Affairs team working remotely or on site from various countries where the company has their offices :UK, Ireland, Hungary, Belgium, Italy, Spain, Lithuania, Poland, Sweden, Norway, Finland, Denmark Czech Republic, Croatia or Romania . It is a permanent role for someone with experience in a CRO and Clinical Research, a professional who would be responsible for authoring Clinical Overviews and Clinical Summaries . The company is very flexible about the location and offers a great financial package and support for its workers!

What qualifications are we looking for

  • Degree in the Life Sciences, Pharmacy, Nursing or a Medicine related discipline
  • Previous CRO or Pharma experience is essential
  • Strong regulatory knowledge of multiple countries is important.
  • Good Regulatory Affairs consultancy experience with a minimum of 2-3 years with a strong background in Clinical Writing (CTD Module 2.5., 2.7)
  • Excellence in English language

What are we offering

  • Flexible type or working Europe-wide with office possibility as well :

  • An excellent salary range

  • Work in an international environment

  • Internal training offer; a stable company

  • Benefit package including healthcare and pension

NonStop is one of the largest and fastest growing specialised life-sciences & Med-tech recruitment companies in Europe. We are proud members of the APSCo life sciences group who ensure we meet the highest quality standards within the recruitment industry. Our offices are located in the UK, Switzerland, Romania, Luxembourg, US and the Czech Republic and we hold labour leasing licences for all EU countries. Please visit our website for a full list of the niche markets we cover.