We are currently partnering with an exciting Biotech company based in Zug who are planning to launch multiple products next year as they expand into Europe from the United States.
Due to a number of products going into phase I, II and III they have a spike in work load so require some support from an experience consultant.
The main area of the role is to prepare and co-ordinate the regulatory documentation to support Clinical Trial Applications/amendments in Europe (Western countries).
- Fluent in English is needed
- Experience managing regulatory submissions with a focus on clinical trial applications
- Must have knowledge of European drug process and regulations
This is an urgent role which can start immediately!