Regulatory Lead, Biologics, Basel
Regulatory Affairs Lead, Early Stage Biologics, Basel, Switzerland
NonStop are currently mandated on a search to find talent in regulatory development for a growing Pharmaceutical company in Basel. The key to this position will be to take the lead for a new portfolio of Biological products. This will cover tasks from early stage development to pre IND/IMPD filings and future submittals. As well as these tasks, the role will also cover being a part of the overall regulatory group and future pipeline products.
I personally find the role very interesting, both for its highly challenging scientific aspects behind it, but also because it is a chance to take a leading role in the regulatory filings. These can quite often prove to be a career defining steps when successful. The company in question have a friendly and open working style, they have already established products and have recently achieved a number of important milestones.
If you would be interested 'in principle', then please contact me and I would be happy to talk through the details of the role prior to any formal commitment.
Report to: CSO
- Leading activities for IND/IMPD filings
- Engage with health authorities and take part in scientific advice
- Help in setting up clinical documents
- Part of the overall regulatory team for pipeline products
- Management of consultants and vendors
- Life science degree
- Over 6 years experience in regulatory affairs
- Experience in regulatory drug development for EMA or FDA
- Fluency in English
For a confidential discussion about regulatory affairs, or to apply, then send your CV to firstname.lastname@example.org or call me, Matt Beedle, Regulatory Affairs Consultant for Switzerland on +41 43 50 80 817 . Please feel free to check my linked-in account for my references.
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