You will be working as the Senior Regulatory Affairs Manager (EU and US markets) and be reporting directly to the Regulatory Portfolio Lead. Alongside their already large portfolio of products both established and in development, they have successfully brought on a new product within the neurology space.
This is an exciting Regulatory Affairs contracting position which will be reporting to the Regulatory Lead and will have you leading regulatory submission strategies, globally. With this role you will be bringing a wealth of expertise with FDA and EMEA interactions. You will be responsible for advising on regulatory strategies for innovative medicines for global markets.
What you'll need to have to be successful in this application:
- Minimum of 8 years Regulatory Affairs Experience
- Direct experience working with FDA and EMEA
- Experience as a strategic lead for submission strategies
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV. Please reach out to Julia Bowden if you have further questions.