IRT Expert (f/m/d)

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 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

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 encourage the implementation of innovative approaches, new technologies and strategies to support the successful completion of supply chain activities Exhibit ability to interpret complex project requirements and ability 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 permanent employment with our business partner Extensive social benefits, incl. Christmas and holiday bonuses Up to 30 days vacation per year