Due to acquisition of a new project by our Client, we are looking for a (Sr) Clinical Research Associate (CRA) who will join an international and innovative life science company based in Austria.

Responsibilities:

  • Site monitoring including close-out of clinical sites, maintenance of study files and writing clinical trial reports
  • Managing site and registry as prescribed in the project plan
  • Traveling to the sites up to 30% of FTE
  • Liaising with vendors, partners and other parties

Requirements:

  • Min. 2-3 years of experience in monitoring clinical trials
  • Experience in clinical research from CRO or a medical device sector would be a plus
  • Degree or equivalent in a life science discipline
  • Fluency in English with knowledge of German

If you would like to find our more, please send your CV with contact details to joanna.osiak@pharmaprofessionals.eu and I will contact you with more information, or please let me know if you may know someone suitable for this role.

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