Upsilon Global

Global Regulatory Affairs Specialist- Belgium

27 Apr 2021
27 May 2021
Regulatory Affairs
Full Time
Contract Type
Experience Level
Experienced (non-manager)

Upsilon Global are working with a mid-size CRO that are growing their team in Belgium. The CRO is a European based CRO that works in various therapeutic areas and in particular in Cardiology studies in both Phases ii-IV and in medical devices. 

The CRO is now seeking a start-up specialist that has experience of at least 1 year in the field to be part of the regulatory and start-up team and working on local submissions and international submissions

Responsibilities include: 

  • Local submissions to Ethics Committees 
  • Regulatory submissions to international submissions
  • Support the team and client with any changes in the laws
  • Working closely with other team members 
  • Working closely with the sponsors 


  • Life Science Degree or similar
  • Min 1 year experience working in regulatory submissions 
  • Experience working for a CRO is preferred
  • Fluent in English 
  • Fluent in Dutch and French




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