Cpl Life Sciences – Regulatory

Director of Regulatory Affairs

Location
Central London / West End
Posted
30 Apr 2021
Closes
30 May 2021
Ref
JO-2103-464598
Contact
Charlie Harris
Discipline
Regulatory Affairs
Hours
Full Time
Contract Type
Permanent
Experience Level
Senior Management

Regulatory Affairs Director
Location: Central London
Salary: Highly competitive salary & package
Job Reference:JO-2103-464598

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.
Responsibilities include.
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
Requirements
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.harris@cpl.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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