Trial Product Handling Process Supporter

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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 your answer is yes, then we have the perfect opportunity for you! The Position The position is in Trial Product Handling; a team of 14 dedicated colleagues responsible for maintaining handling temperature deviations in clinical trials, IRT systems, quality/training support and general trial product handling support to affiliates and clinical sites globally. 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
  • Conducting and creating training
  • Temperature monitoring devices (ship and storage) – calibration and vendor management
  • Providing support regarding calibration certificates
    • 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 everyday 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 or engineering. In addition, you have:
  • Quality mindset and ideally have experience working within GxP regulated processes in the pharmaceutical industry
  • Sense for the detail and prefer to work in a structured way
  • Preferably, experience as either a Process Supporter in a production/quality assurance department or from the clinical area
  • Knowledge how to navigate in a GMP/GDP/GCP regulated field and with several stakeholders involved daily
  • Skills within written documentation is a pre-requisite because documentation is an important part of the job
  • Fluent knowledge in English is a must, Danish is nice to 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. Working at Novo Nordisk At Novo Nordisk, we don’t wait for change. We drive it. 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. From research and development, through to manufacturing, marketing and sales – we’re all working to move the needle on patient care. Contact For further information, please contact Katrine Elkjær Mønsted, +4530756956 Deadline 6 August 2023 You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.


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    Denne ledige stilling har jobtypen "Forretningsudvikler", og befinder sig i kategorien "Kommunikation, marketing, salg".

    Arbejdsstedet er beliggende i Måløv.

    Jobbet er oprettet på vores service den 28.4.2023, men kan have været deaktiveret og genaktiveret igen.

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    Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
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