Your Tasks: Define, develop, and establish global supply for clinical trials (Phases I to IV) with internal departments. Monitor clinical care requirements and procure necessary materials, including comparators. Manage bookings and tasks in IRT systems (including UAT). Review manufacturing and packaging regulations, batch protocols, specifications, and SOPs with quality assurance, regulatory affairs, and clinical trial management teams. Ensure GxP compliance, develop SOPs, and improve global clinical trial supply processes. Represent the Clinical Trial Supply (CTS) division to stakeholders. Support supplier selection, contract management, and budget preparation for projects. Your Profile: 2-3 years experiences in oncology clinical trials supply. 2-3 years of experience in a GxP environment, preferably in the (radio)-pharmaceutical or medical technology industry. Knowledge of European and US GMP requirements for labelling, packaging, and distribution of investigational medicinal products (GCP experience is a plus). Strong teamwork, problem-solving, and communication skills. Flexibility, organizational talent, and customer/result orientation. Willingness to travel internationally (approx. 10%). Proficiency in MS Office applications (especially Excel). Fluent in German and English.