Clinical Safety Specialist - Maastricht

Function Group: Clinical Research / Clinical

Organization

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.

Function

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.

Requirements

  • Clinical research experience
  • Medical background
  • Resilience
  • Curiosity
  • Teamspirit

Application

If you are interested in this job, or in similar ones, please feel free to contact me directly.

Rick Venneman

Manager Medical Devices division

+31(0)23-7548660
+31(0)6-40916403

r.venneman@qtcrecruitment.com

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