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• ITech Consult AG
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• ITech Consult AG
• Write an email

• Support GxP compliance of all activities in the clinical trial supply management, drug-related distribution and storage
• Responsibility for the project-related GxP documentation and maintenance of lists

Support of planning, managing and steering of timelines, costs and scope of Trial Teams for agreed deliverables of global supply chain activities for assigned clinical trials, including highly complex trials...

Identify and evaluate adjacent business opportunities, changing clinical practices, unmet needs, reimbursement developments, future healthcare trends, and emerging digital technologies....