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* DevelopIRT 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
* SelectIRTVendorandcreatestudyspecificcontract
* Conductand documentValidation/User Acceptance Test activities
* Performregular maintenance of the IRT system to adjust for trial needs, additional requirements after go-live etc, in collaboration with the study team
* Utilizeagile and proactive approach and innovative technology to solve problems
* Supportthe successful setup of the supply chain and patient management activities through the use of IRT
* Ensurethat all work is performed according to GxP and conforms with US, EU and other international regulations
* Workindependently and in an international, cross-culture team environment
* Master's degree with several years of professional experience
* Proven ability to drive results in a changing environment and to discuss and present proposals in a concise and effective manner
* Ability to learn new technologies and concepts to enhance operations
* Strong problem solving capabilities and encouragethe implementation of innovative approaches, new technologies and strategies to support the successful completion of supply chain activities
* Exhibitability to interpret complex project requirementsand provideability to interpret highly complex experimental data and project requirements
* Solid project management skills including presenting projects and status reports to different audiences
* Fluent in English with excellent written and verbal communication skills
* Option of permanentemploymentwithourbusinesspartner
* Extensive social benefits, incl. Christmas and holiday bonuses
* Up to 30 days vacation per year