Description
Senior Regulatory Associate - Leading Global Pharma - Pre approval Oncology - Up to £50,000 basic - UKSenior Regulatory Associate - Leading Global Pharma - Pre approval Oncology - Up to £50,000 basic - UK
We are currently working with a leading global pharmaceutical company who are currently looking to expand their drug development team. They currently have a need for a Senior Regulatory Associate to help support their oncology division and to work on products in both development and established, to enhance their European presence. You will be joining a forever expanding company with opportunities to build a promising career and you will have the opportunity to work on their highly interesting oncology portfolio.
Key Skills/Requirements
- University degree - medical or paramedical
- 2-5 years experience in regulatory affairs
- Strong pre approval regulatory experience (not just clinical trials)
- Phase II and III experience
- Post approval experience desirable
- Involvement in European regulatory strategy
- European regulatory experience
- Oncolgy experience desirable
- Project management skills
The company is continuously growing and encourage applicants with strong career ambitions to apply for the position. They are looking for strong self starters, candidates who have hands on experience of the drug development process and people who have the ability to make a difference within the regulatory team.
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