Job Description

EU Submission Hub

Søborg, Denmark

Are you looking for an exciting opportunity where you can make a real difference? Would you like to join a dynamic international team where no two days are the same? If you thrive in a collaborative environment across cultures, this could be your next career step.

Your new role

As a Regulatory Submission Professional, you will play a critical role in managing and coordinating clinical trial submission activities within the EU. You will work in a fast-paced environment with multiple stakeholders and tight timelines, ensuring high-quality and compliant submissions.

Your main responsibilities will include:

  • Working on process optimization for CTA submissions within a team and stakeholders from other teams 
  • Working closely with various submission teams across the organization and all countries in Europe
  • Managing initial clinical trial application submissions in the EU according to...

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