Clinical Supply Coordinator | Koordinator (m/w/d) klinische Versorgung (1421)
Brüggen Engineering GmbH
Job Summary
As a Clinical Supply Coordinator in the innovative pharmaceutical industry, you will be a key figure in organizing and providing clinical trial samples for global studies based in Ludwigshafen am Rhein. Day-to-day responsibilities include actively supporting the Project Manager in planning and logistics, coordinating standardized activities across global clinical trials, managing orders for packaging and labeling, and ensuring compliance through active participation in shelf-life extensions. A crucial part of the role involves developing new strategies to optimize clinical sample provision and supporting the creation and revision of GMP/GCP-relevant Standard Operating Procedures (SOPs). This role requires a background in Natural Sciences or Healthcare, foundational project management knowledge, and initial experience in pharmaceutical development or a regulated GMP/GCP environment, making it an excellent opportunity for professionals seeking a career combining organization and innovation.
Required Skills
Education
Completed degree in Natural Sciences, Healthcare, or a comparable qualification.
Experience
- Initial experience in pharmaceutical development
- Initial experience in the GMP/GCP environment
- Basic knowledge of Project Management
Languages
Additional
- Knowledge of GMP and GCP regulatory requirements.
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