Switzerland, Regulatory Affairs Associate Director RA_AC_13655-MZ
ProClinical has partnered exclusively with a Swiss-based biotech specialising in a range of therapy areas.
My client is seeking an RA Associate Director to join their team in La Suisse Romande to focus on leading two new indications in anti-infectives. There will also be the opportunity to work across other therapy areas including Oncology in the future.
The role will focus on leading 2 indications through clinical development (Phase II-III) and dealing with the FDA. Other responsibilities will focus on developing global RA strategy and leading submissions including CTA/INDs, ODD, PIP/PSPs etc.
The ideal candidate will have a solid background in Regulatory Affairs, ideally with an innovator pharmaceutical company/biotech. Global submissions/strategy experience is desired as is Fluent English and ideally French as well.
Applicants must be EU-based.
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