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Senior Manager, Regulatory Affairs

Central London   •  Negotiable  •  Permanent, Full time


Senior Manager, Regulatory Affairs

London (Hybrid)

Up to 70,000

Senior Regulatory Affairs Manager position working for a global pharmaceutical company that works across a range of different therapeutic areas including the central nervous system, Infectious Diseases, Pain, and Womens Health.

You will be responsible for managing EU submissions for products going through development and post-marketing activities. Including working across MAAs, CTAs, preparing documents for Scientific Advice and PIPs.As a Senior Regulatory Manager, you will be responsible for dealing with the health authorities including supporting regulatory submission strategy.

Responsibilities:

Supporting post-marketing licensing requirements and ensuring effective liaison across the organisation to optimise regulatory strategies.

Supports the preparation of key regulatory documents (e.g. MAAs, CHMP Scientific Advice, PIPs) and responses to questions from Health Authorities.

EU focused role.

Requirements:

Previous experience working on pre and post-approval.

Innovative product background.

University degree in Life Sciences.

Minimum 5 years of experience in Regulatory Affairs within the pharmaceutical industry.

The role is an excellent opportunity to gain further exposure within development and pre-approval. The role will be a hybrid position with two days of office work (London) per week.

This role comes with an excellent package including a car allowance, bonus, and long-term incentive schemes.

For more details please contact lucy.kirkaldy@cpl.com

  • Agency: Cpl Life Sciences
  • Reference: JO-2209-500806
  • Posted: 13th September 2022
  • Expires: 11th October 2022

Cpl Life Sciences

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