Clinical Supplies Set-up Specialist

3 weeks ago


Ballerup, Ballerup Kommune, Denmark Novo Nordisk Full time
About the Role

We are seeking a highly skilled Clinical Supplies Set-up Professional to join our team at Novo Nordisk. As a key member of our Clinical Supplies Trial Set-up department, you will play a crucial role in preparing clinical trials for supply execution.

Main Responsibilities
  • Ensure clinical supply input to clinical trial protocols is accurate and up-to-date.
  • Create trial master data, clinical label text, and trial-specific manuals to align with product specifications and regulatory requirements.
  • Ensure documents are ready for clinical trial application to authorities.
Qualifications
  • MSc degree in Natural, Health, or Pharmaceutical Sciences or similar.
  • Experience in the pharma industry is a plus.
  • Quality mindset and experience with regulatory requirements, such as GCP and GMP.
  • Data-driven, analytical, and methodical capabilities with flair for IT systems and tools.
  • Excellent collaboration and communication skills with fluency in English.
About the Department

The Clinical Supplies Trial Set-up department consists of six teams who prepare clinical trials for supply execution by forecasting product demand, simulating trial supply execution, setting up supply systems, and preparing regulatory documents for CTA.

Working at Novo Nordisk

We're a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them.



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