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.
Please visit our website at www.proclinical.com