Trial Product Handling Specialist

Do you have a desire to set direction for processes around Trial Product Handling at clinical sites globally which is essential for the Novo Nordisk’s clinical trials? Are you eager to learn about how Novo Nordisk develops and run Clinical Trials? If your answer is yes, then we have the perfect opportunity for you!

The Position

The position is in the department Supply Chain Planning. You will be responsible for various tasks related to Trial Product handling with focus on the temperature deviation process, temperature loggers and GCP requirements related to IRT systems, but also shipments, receipt, storage, destruction etc.

You will be responsible for requirements in our global procedures for Trial Product Handling and be responsible for:

All things related to supporting and improving to the benefit of the Clinical sites and our colleagues in the affiliates who are responsible for overseeing the trials daily.

Your contribution will ensure that all our almost 5000 clinical trial sites all over the globe are being supported in the most optimized and efficient way. You will have a direct impact on how we run clinical trials and will be involved in many important processes. In addition, you will become part of a very engaged and highly skilled team where every day will provide challenges and opportunities for learning and growth. You will work with colleagues with whom you can both learn from and have fun with.

Qualifications

You hold a master’s degree within pharmaceutical sciences, engineering or similar.

In addition, you have:

You seek simple and effective solutions and see continuous improvement as a natural part of processes and are familiar with various LEAN principles. You are a team player and find motivation when reaching common goals.

About the Department

You will join Supply Chain Planning which is a part of Clinical Supplies in CMC Development. We are responsible for the overall planning of the production, packaging, and distribution of products for Novo Nordisk clinical trials worldwide. The department consist of four teams, supporting the execution of clinical trials by forecasting and monitoring product demand, ordering products/materials, planning the packaging and shipping of trial products and supporting the overall trial conduct at the clinical sites with a focus on trial product related processes and systems. You will be reporting to the director of the Supply Chain Planning department and be a part of the department leadership team.