Clinical and Regulatory Affairs Consultant

vor 1 Woche


PlanlesOuates, Schweiz SpineArt SA Vollzeit
Clinical and Regulatory Affairs Consultant

Do you want to work for an innovative specialist spinal implant company and play a pivotal role in advancing medical research?

If yes, come to join our clinical studies team as Clinical and Regulatory Affairs Consultant

(2 years mission - min 20 hours per week)

Your main responsibilities will be:

  • Managing clinical evaluations by planning and leading the process with third party clinical evaluation authors.
  • Developing a streamlined and consistent process.
  • Supporting clinical submissions to regulatory bodies, developing clinical regulatory strategy, and creating Post Market Clinical Follow-up plans and Summary of Safety and Clinical Performance (SSCPs) documents.

Your profile:

  • Over 5 years of experience in clinical evaluation writing, ideally in the orthopedic field, focusing on spine surgery.
  • Qualification in a clinical or medical field.
  • Advanced knowledge of the EU 2017/745 MDR regulatory framework.
  • Fluent in French and English.

We look forward to receiving your application at:

Apply Here

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