About this role

  • Posted on

  • Location


  • Salary

  • Type


  • Division

    Pharmaceutical Regulatory Affairs Jobs

  • Reference

    BB - 12776.5_1599119443

  • Start date


  • Managing this role

Executive Consultant

Brieuc Baeckeroot

+44 203 8540 263


Source Group International GmbH, Bosch 106, 6331 Hunenberg, Switzerland


As Global Regulatory Lead, you will take over a project and work with cross-functional teams. From the Clinical research to the life cycle Management you have a full overview of the process to define the best possible strategy.

By leading the strategy from its implementation to the execution will allow you to develop your skills on different levels: From the regional area to the product’s stage, as well as the transverse management. This is a great opportunity to develop your technical and personal competencies to evolve in your career.

Your task:

  • You will be the man point of contact regarding the Regulatory question: Strategy, risk assessment for the project.
  • Leading the cross-functional team in order to work toward a common goal and meet the key milestones
  • Accountable for the strategy design, its development, and implementation
  • Review the final/key documents prior to their submission

Your experience:

  • 7 Years of experience in the Pharmaceutical Industry.
  • Having an experience/knowledge of the Global Regulatory procedure from the clinical development to the Life cycle Management
  • Good track record in terms of delivering Regulatory Approvals
  • You worked across several teams or in a multi-teams environment

Do you think you would be a good fit? Do you want to know more about the role? Do not hesitate to contact me.


Feel free to reach me even if the position is not exactly what you are looking for.
Please share it with your network or any person you think you might be interested in.

You can send me your CV, Resume with your contact details through the link OR you can contact me on Linkedin.

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