Clinical Supply Manager

Grünenthal Group

Aachen, Germany

Purpose of the role:

Project Management of clinical trial supplies for global phase I - IV studies from demand planning to QP release of packaged trial medication and logistics reflecting applicable GxP requirements.

Your responsibilities:

  • Ensuring an un-interrupted supply chain is maintained throughout the study through new packaging campaigns and shelf-life updating activities;
  • Central point of contact for all medication related activities for an individual project and/or individual trial;
  • Coordination of manufacture of clinical trial medication (e.g. planning, coordination of bulk manufacture, packaging and labeling, coordination of QP release and storage);
  • Setup of trial specific Interactive Response Technologies (IRT) system;
  • Setup of the logistical trial-specific supply chain;
  • Coordination of tasks related to operational logistics of trial medication in close collaboration with the Global Operations Study Leader and the Outsourcing and Contract Manager;
  • Monitoring of clinical supply inventory to ensure proper control over stocks at Grünenthal or partner warehouses;
  • Ensure implementation of adequate shipment conditions.

Your profile:

  • Degree as pharmacist or comparable scientific qualification (e.g. MSc, Diploma, PhD);
  • Experience in clinical trial supply management of global clinical trials;
  • Experience in the setup and use of Interactive Response Technologies (IRT);
  • Thorough understanding of GxP requirements, i.e. Good Manufacturing Practice, Good Distribution Practice and Good Clinical Practice;
  • Advanced communication skills and focused mindset;
  • Service-oriented and enjoy working in interdisciplinary teams;
  • Excellent analytical and organizational skills;
  • Fluent in English (verbal & written).

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