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Description

The CTA will assist in the conduct of Clinical trial activities such as to support in submission process, to ensure appropriate documentation and to prepare relevant trial specific documents and communication with trial sites. This position is a part-time position (30 hours/week) for one year and located in Jena.

Tasks

  • Support in Conduct of clinical studies and registries according to all applicable regu-lations, to commonly accepted practices, and to Occlutech’s internal guidelines
  • Preparation and Maintain Sponsor File
  • Preparation of study-specific documents
  • Support Clinical Project Management in any study activities
  • Track record of Study Document
  • Prepare and documents Meetings
  • If required, assist in Study audits
  • Perform other related duties and responsibilities, on occasion, as assigned

About Occlutech

Nach Gründung in Deutschland im Jahre 2003 ist Occlutech bis heute eines der führenden Unternehmen auf dem Gebiet der strukturellen Herzkrankheiten geworden. In mehr als 80 Ländern werden ASD, PFO, LAA, PLD und PDA Occluder sowie Zubehör und ein Sortiment an innovativen speziellen Herzimplantatprodukten entwickelt und vertrieben.Mit mehr als 50.000 eingesetzten Implantaten ist Occlutech über ein eigenes Vertriebssystem in Deutschland, Großbritannien, Italien, Frankreich und in Skandinavien sowie über ein starkes Netzwerk mit Vertriebspartnern in der restlichen Welt vertreten. Occlutech verfügt über eigene F&E- und Produktionsstätten in Deutschland, Schweden sowie in der Türkei. Dies erlaubt neben einem schnellen Wachstum flexible F&E-Leistungen und effiziente und rationelle Fertigungsprozesse, die sicherstellen, dass die Produkte bezahlbar bleiben und zugleich neue Investitionen in die Forschungs- und Entwicklungspipeline des Unternehmens ermöglichen.
» learn more about Occlutech

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