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Job Details


Job Details

Ihre Aufgaben

  • Develop IRT System specifications to meet the needs of the study design in collaboration with Clinical Trial Supply Unit (CTSU) functions, Medical, Clinical Data Management and Biostatistics
  • Select IRT Vendor and create study specific contract
  • Conduct and document Validation/User Acceptance Test activities
  • Perform regular maintenance of the IRT system to adjust for trial needs, additional requirements after go-live etc, in collaboration with the study team
  • Utilize agile and proactive approach and innovative technology to solve problems
  • Support the successful setup of the supply chain and patient management activities through the use of IRT
  • Ensure that all work is performed according to GxP and conforms with US, EU and other international regulations
  • Work independently and in an international, cross-culture team environment

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