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Senior Associate Regulatory Affairs

West London   •  £25 - £32 per hour  •  Contract/Temporary, Full time

Our client, a global pharmaceutical company, is currently looking for a Senior Regulatory Affairs Associate to join their team. 

Key Responsibilities

  • Contribute to the creation and submission of regulatory documents, particularly to those associated with clinical trials, and ensure these are presented in a timely manner to the regulatory agencies
  • Gather all regulatory documents needed for applications and ensure that a record of it is kept
  • Provide and maintain CTA/MA documentation support.
  • Support regional regulatory pre-filing activities.
  • Ensure that all procedures adhere to Regulatory guidelines
  • Maintain an active awareness of EU and EEMEa Regulatory legislation


  • Previous experience in Regulatory Affairs and Compliance particularly within the pharmaceutical industry
  • Must have CTA and EU affiliate experience.
  • Exposure of Regulatory Affairs legislation and procedures
  • Strong communication and interpersonal skills

For more information, please contact me on 01727 817600 or fhatib@achieva.co.uk

  • Agency: Achieva Group Limited
  • Contact: Fandi Hatib
  • Phone: +44 (0)1727 811 634
  • Reference: 32160
  • Updated: 27th September 2021
  • Expires: 25th October 2021

Achieva Group Limited

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