Middle 1000 – 5000
Regulatory Affairs / /
– Experience in working with EMA (including CTA, NTA, ODD, PRIME, scientific advice and other relevant regulatory
– 5 to 10 years experience minimum
– Fluent in English
– MD / PharmD background
The client is a biotech company looking for a Regulatory Affairs Interim Manager in the perspective of a product launch before a potential permanent hiring.
Your role will be :- at the interface between the company and the regulatory authorities, through the entire life cycle of the medication, from early development, to commercialization.
– to inform and direct the development and commercialization
– to be the internal regulatory affairs expert.
Experience 5 – 10 years,Experience > 10 years
FTE / nb of days per week
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