Science, Pharmaceutical & Food

Regulatory Affairs Senior Manager

  • Contract
  • Remote
  • Greater London
  • 41896598

PE Global is currently recruiting a Regulatory Affairs Senior Manager for a 12-month contract role with a leading multinational Biopharma client based in London.

Job Responsibilities

  • Support planning, preparation, and submission of clinical trials as well as other Health Authority Interactions in Europe and Globally.
  • Provide operational and strategic insight to the project team regarding product development in Europe.
  • Manage post approval activities to support product license and life cycle activities
  • Communicating with regulatory consultants and CROs regarding product development plans
  • Manage interactions and relationship with Health Authorities in Europe or other regulatory authorities as assigned


  • Background in the pharma industry is essential.
  • Proven ability to manage critical projects as a part of an interdisciplinary team with significant experience in managing clinical trial submissions.
  • Preferable to have experience interacting with regulatory authorities, including help the preparation for key regulatory meetings.
  • Prior experience managing regulatory submissions to ensure successful in time submissions to support the strategic and operational objectives.
  • Thorough understanding of relevant drug development regulations and guidelines.

Interested candidates should submit an updated CV.
Please click the link below to apply, call Veronica on +44 203 868 9000 or alternatively send an up to date CV to

***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in UK***

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