Switzerland, Associate Director EMEA RA_NW_13663-MZ
ProClinical have partnered exclusively with a Swiss-based biotech specialising in a range of therapy areas. Our client is seeking a dynamic Regulatory Affairs Associate Director to join their team in Switzerland where you will be responsible for development & execution of EU submission strategy for assigned projects.
The ideal candidate will have a solid background in Regulatory Affairs, ideally within in an innovative pharmaceutical company/biotech. Strong EU submissions/strategy experience is required as well as good cross-functional leadership capabilities. Fluent English is required and ideally French as well.
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