Novo Nordisk
Trial Product Handling Professional
Do you have a desire to support processes around Trial Product Handling at the 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 Yes, then we have the perfect opportunity for you!
The Position
As a Trial Product Handling Professional you will be responsible for various tasks related to Trial Product handling with focus on the temperature deviation process. You will get hands-on experience in the process of evaluating temperature deviations to be able to support the process best possible and will also be responsible for:
Updating procedures
Writing deviations and change requests
Providing support regarding to the temperature processes
All things related to supporting and improving to the benefit of the Clinical sites and our colleagues in the affiliate which is 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
To succeed in this role, you have:
A master’s degree within pharmaceutical sciences or engineering
Experience working within GxP regulated processes in the pharmaceutical industry
Experience as either a Process Supporter in a production/quality assurance department or from the clinical area will be a plus
Experience within documentation
Good communication skills in Danish and English.
You have a quality mindset, and know how to navigate in a GMP/GDP/GCP regulated field and with several stakeholders involved daily. You have sense for the detail and prefer to work in a structured way.
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 five 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.
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