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Medical Device – Scientific Adviser – Regulations

We have a fantastic opportunity available as a Senior Manager of Clinical Evaluation at a Global Medical Device company based in Southern Germany. This is a fantastic opportunity for a scientifically and academically minded individual to enter into an important position in a brand new team.

Role Responsibilities
Interpret data and literature surrounding clinical safety and performance of the medical devices
Investigate and evaluate whether the available data has an impact on the risk profile or existing overall clinical assessment of the product
Conducting literature research and contribute with expert opinion on post-market surveillance and Risk Assessment
Production of documentation to update existing technical documentation
Construction of Clinical Evaluation Reports

Experienced Required
PHD or greater academic qualification
Interest in the Medical Device area
English speaking

This opportunity has understandably been incredibly popular. We encourage all interested candidates to apply without delay as it is likely that recruitment will close prematurely. Please direct all questions (if necessary) to “Simon” at strebilcock (at) barringtonjames (dot) com alongside a copy of your CV.

Closing Date:

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