Director of Regulatory Affairs
- Experience Level
- Senior Management
Regulatory Affairs Director
Location: Central London
Salary: Highly competitive salary & package
CPL Life Sciences are supporting an innovative and forward-thinking pharmaceutical company in London to hire a strategic EU Regulatory Affairs Director. This position will oversee EU regulatory activities for both developing and marketed products and have overall responsibility for submission strategies.
Leading the preparation of key regulatory documents (e.g. MAAs, CHMP Scientific Advice, PIPs)
Supporting post-marketing licensing requirements
Managing CTA strategies and the CTA submission process
Assisting with the preparation for communication with Health Authority inspections and independent audits
10+ years experience working within Regulatory Affairs.
Must have worked with centralized procedure applications.
Must have a technical and strategic mindset.
Must be experienced working with clinical development activities scientific advice, PIPs etc.
If you are interested in discussing this role or any of our other active positions, please dont hesitate to contact me at Charlie.email@example.com.
Remember if this role is not suitable for you please feel free to forward this to anyone you feel would be suitable. If we successfully find a role for your recommendation we will give you 250 in vouchers of your choice.
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