Your new company
Global Biotechnology in the UK are looking for a Regulatory Affairs Manager to develop and implement regulatory strategies for EU markets for their Oncology portfolio. This position will sit within the global regulatory team and will require someone to have both development and post-marketing experience.
Your new role
This role will support one or more products from a regional (EU) regulatory perspective. As a member of the GRT, you will ensure that the company acquires and maintains approvals to support clinical trials for products as well as for market approved medicinal products. You will be supporting the senior management team with the execution of regulatory strategies for the oncology portfolio.
What you'll need to succeed
You must have experience with CTA's and CTR for the EU. You will have extensive experience with innovative medicine working from development phases through to post-marketing. You will also need to be on a 1 month or less notice period.
What you'll get in return
This role is 12 months in length with scope for extension. The team meets up once per month in Uxbridge/Cambridge.
What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.If this job isn't quite right for you, but you are looking for a new position, please reach out to Julia Bowden for more details.