SciPro have partnered with an innovative pharmaceutical company based in the UK with an office in reading. They are looking to add a Senior Regulatory Affairs Manager to their team. They are known for producing ground breaking drug delivery methods that will revolutionise the way neurological conditions are treated and viewed world wide.
As their regulatory manager you will be working directly with the global medical director / head of regulatory affairs to provide input when it comes to orphan indications as well as license transfers
- Orphan drug indications
- License transfer / registration
- Project management
To apply click below!