* 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.
