For a leading and fast-growing medical device company with a global presence, we are looking for a Clinical Safety Specialist on short notice. The company operates in more than 400 locations all over the world. They are performing multiple clinical studies worldwide and are located in Limburg, the Netherlands.
As a Clinical Safety Specialist, you will be responsible for reviewing and reporting the adverse events patients experience. You will also check the adverse event for completeness, seriousness, procedure and clarity. You will, furthermore, be responsible for assessing whether the AE needs to be reported. Thereby, you will organise meetings with medical doctors. You will have a close collaboration with different Stakeholders and RA, Vigilance and Clinical Study Teams. Additionally, you will be part of the safety team, which is a global team supporting more than 100 studies in more than 10 business units.
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Manager Medical Devices division