Clinical Supplies Specialist
4 weeks ago
Are you passionate about clinical trials and ensuring the smooth execution of clinical supplies? We are seeking a dedicated Clinical Supplies Specialist to join our team at Novo Nordisk. If you have a strong background in natural, health, or pharmaceutical sciences and experience in the pharma industry, we encourage you to apply for this challenging role.
The Position
As a Clinical Supplies Specialist, you will be responsible for ensuring clinical supply input to clinical trial protocols, creating trial master data, and ensuring documents are ready for clinical trial application to authorities. You will work closely with a wide range of stakeholders across Novo Nordisk and be empowered to develop and improve processes.
Qualifications
To succeed in this role, you will have a MSc degree in Natural, Health, or Pharmaceutical Sciences or similar, experience in the pharma industry, and a quality mindset with experience with regulatory requirements, e.g., GCP and GMP. You will also have data-driven, analytical, and methodical capabilities with flair for IT systems and tools, excellent collaboration and communication skills, and 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.
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Clinical Supplies Specialist
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Ballerup, Ballerup Kommune, Denmark Novo Nordisk Full timeAbout the RoleWe are seeking a skilled Clinical Supplies Specialist to join our team at Novo Nordisk. As a Clinical Supplies Specialist, you will play a critical role in ensuring the smooth execution of clinical trials.Main ResponsibilitiesEnsure clinical supply input to clinical trial protocolsCreate trial master data, clinical label text, and...
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Clinical Supplies Set-up Specialist
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