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* Support of planning, managing and steering of timelines, costs and scope of Trial Teams for agreed deliverablesof global supply chain activities for assigned clinical trials, including highly complex trials (e.g. Mega trials, adaptive trial design, digital trials, trials fully outsourced to a third party (CRO)and Investigator Initiated Studies (IIS), EAP as well as NPU programs)
* ResponsibletosupportTrial Managers for theautonomousmanagementof theCTSUtrialteamwithinthematrixstructure
* Support of CTS preparation documentation
* Support ofteammeetings,minuteswithactionpointsandresponsibilities
* Support of different systems like BIRDS (BI System) administration and workflows, Focus entries/updates, CESentries/updates, AC Evaluation coordination, AC Ordering, MLT drafting prior to TrM review/approval, GTLmaintenance, manuel release form as well as manuel shipping request for bulk shipments, stability samples and sampling documentation for Investigational Medicinal Products
* Bachelor's Degree with some years of experience
* Relevant experience in Pharmaceutical industry
* Basic project management skills
* Broad and thorough knowledge and understanding of applicable US and EU regulations and other internationalregulations
* Strong problem solving capabilities and encouragethe implementation of innovative approaches, new technologies and strategies to support the successful completion of supply chain activities
* Proven ability to drive results in a changing environment and to discuss and present proposals in a concise andeffective manner
* Strongcomputerskills(e.g. Microsoft Office 365, Project Management Software)
* Ability to present projects/status reports to different audiences
* Very good to fluent in English, spoken and written
* Excellent written and verbal communication skills
* Willingness to travel
* Option of permanent employment with our business partner
* Up to 30 days vacation per year
* Option of permanent employment with our business partner