For our Clinical Trial Supply department, in Marburg, Bern, Zürich or King of Prussia, we are looking for aGlobal Planner, Clinical Trial Supply (m/f/x)R-251735Fulltime / permanent / tariffInternal job title: Global Planner CTS Supply Chain Internal closing date: 08.04.2025The OpportunityMonthly Forecast Planning and updating on study specific Demands in close cooperation with Study Managers and CMCCreation and maintenance of delivery schedules (Supply) for clinical goods in close cooperation with CSL global and regional product planners and CMOsRecording of the requirements planning in the global CSL planning tool (RapidResponse), ensuring and tracking the transfer of quantities to SAP S4 HanaCoordination of a timely and complete delivery of all clinical studies by CSL Behring worldwide with the required test goodsParticipation and initiation of international task force meetings as CTS representatives to coordinate requirementsCreation and maintenance of material master data in MDGMaintenance of the central Forecast Entry Sheets (planning tool from CTS Planning)Provision of data for Study Managers, Packaging & Labeling Teams, CMC, CMOs, etc.Preparation, execution, and documentation of monthly Forecast MeetingsInitiation, coordination and monitoring of the transport of clinical goods between the CSL manufacturing sites, CMOs and to external service providers worldwideRegular coordination with external service providers about the quantities required and the stock situationCoordination of complete and timely deliveryMonitoring and management of material stocks at external service providersEnsuring the provision of delivery and inventory reports from external service providersSupport in forecasting and budgeting for product costs and variancesCollaboration in the development and review of SOPs, forms, and templates, as well as in the global change management processKnowledge of international guidelines (GCP, GDP, GMP) and official requirements, requirement plans, global and local CSL guidelines and SOPs, manufacturing and testing processes, contracts, procedural instructions and quality agreements Your Skills and ExperienceUniversity degree (BSc, MSc) in life sciences, engineering, logistics or equivalent experience5+ years' experience in clinical research and/or clinical supply management or global R&D project management in the pharmaceutical industryKnowledge of ICH-GCP regulations and the conduct of clinical studiesKnowledge of cGMP and cGDP regulationsWhat we offerHybrid working models. Learning opportunities with our CSL Academy. Global and diverse environment with modern workspaces. Up to two additional leave days for your personal wellbeing. For more information, please check out our global benefits belowWe are looking forward to your application. Please ensure to apply online with your CV and certifications as well as your salary expectation.Our BenefitsWe encourage you to make your well-being a priority. It’s important and so are you. Learn more about how we care at CSL.About CSL BehringCSL Behring is a global leader in developing and delivering high-quality medicines that treat people with rare and serious diseases. Our treatments offer promise for people in more than 100 countries living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. Learn more about CSL Behring.We want CSL to reflect the world around usAs a global organisation with employees in 35+ countries, CSL embraces diversity and inclusion. Learn more about Diversity & Inclusion at CSL.Do work that matters at CSL Behring!