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Senior Medical Writer – part time


You will be responsible for writing the clinical evaluations and post market clinical follow-up (PMCF) files, including for example systematic literature reviews, and assessing technical documentation.

There is increased focus on our area of expertise, and we are seen as a valuable and essential part of the device life cycle. Boiled down, we provide the clinical evidence that our devices are safe to use and perform the way they are required to, so our users can receive the best help possible to aid their hearing loss.

Anja, Manager of the Clinical Affairs team

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