Coordinator Clinical Supply | Koordinator (m/w/d) klinische Versorgung (1421)

Job Summary

As a Clinical Supply Coordinator, you will be a pivotal figure in the pharmaceutical industry, based in Ludwigshafen am Rhein, Germany. Your primary responsibility will be to support the planning, organization, and coordination of clinical trial material provision for global studies. This involves actively assisting the Project Manager, coordinating standardized activities within international clinical trials, and managing orders for packaging and labeling of trial materials. You will also contribute to the extension and revision of clinical trial materials to ensure their availability and compliance. A key aspect of the role is developing new strategies to optimize clinical trial material supply and presenting these concepts to project teams. Additionally, you will support the creation and revision of GMP- and GCP-relevant Standard Operating Procedures (SOPs), ensuring regulatory adherence and quality. This role is ideal for someone with strong organizational skills, a scientific background, and a desire to contribute to making pharmaceutical supply more efficient and successful.