Posted to MedZilla on 1/17/2020


Switzerland, Regulatory Affairs Associate Director - Contract RA_PD_13656-MZ


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.

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 Peter Duvall on +44 203 0789 542 or upload your CV on our website -
A full job description is available on request.
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