Clinical Supplies Specialist

1 month 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.

Key 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.
Requirements
  • 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, e.g., 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 Us

At Novo Nordisk, we drive change and strive for excellence. We're a dynamic company in a 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 experimentation, prioritize patient care, and recognize the importance of diversity and inclusion.

What We Offer

We're committed to creating an inclusive culture that celebrates diversity, promotes equality of opportunity, and fosters a collaborative work environment. If you're passionate about clinical trials, have a quality mindset, and are driven to deliver high-quality work, we encourage you to apply for this exciting opportunity.



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