Clinical and Regulatory Affairs Consultant
vor 1 Woche
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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