Posted to MedZilla on 2/16/2020


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.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please call Nicholas Walker on +44 207 4400 678 or upload your CV on our website -
A full job description is available on request.
ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. 

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  considered, please do so. Applications for all positions are subject to each employer's specific requirements.