Description
Senior Regulatory Affairs Scientist - Leading European Consultancy - Developmental Biologics Experience - Up to £60,000Senior Regulatory Affairs Scientist - Leading European Consultancy - Developmental Biologics Experience - Up to £60,000
I am currently working with a reputable Global Consultancy who are looking to expand their regulatory affairs team. Due to a high demand in developmental biological projects there is a need for a senior regulatory specialist to join the team. The team consists of highly experienced regulatory professionals with over 25 years experience and therefore this is a great opportunity to work alongside the best of the best and develop your already specialist skill set. The company collaborate with start-up, medium-size and large pharmaceutical companies to bring products to the market in the most efficient and cost-effective manner and this is a chance for you to be a part of this framework.
Key skills/Requirements
- 5 - 10 years regulatory affairs experience
- Strong experience in biologic development regulatory
- Strong pre approval experience
- Phase II and III experience
- CTA experience
- Previous experience compiling and submitting an MAA
- Experience of leading your own projects (no line management experience needed)
- Strong European experience
- New Drug Applications (NDAs)/Biologic License Applications (BLAs), Investigational New Drug Applications (INDs) and/or Orphan Drug Designations (ODDs) experience needed
This is a great opportunity for someone to deepen their regulatory expertise. The projects this consultancy takes on are always exciting and interesting and gives you the opportunity to diversify and broaden your experience.
If this is of interest to you and you would like to find out more information on this position or any other regulatory affairs positions, please contact Amanda Edwards on or please email a.edwards(a)realstaffing.com
To find out more about Real please visit www.realstaffing.com