Coordinator for Clinical Trial supplies
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Do you have flair for and a desire to take on the responsibility for setting up an IT system that is essential for the logistics of our clinical trials? If Yes, then we have the perfect opportunity for you! We are right now looking for a talented individual to join our team in Clinical Supplies. As part of Novo Nordisk’s R&D family, CMC Development makes a real difference for patients with chronic diseases across the world. We develop, manufacture and distribute drug candidates for all Novo Nordisk non-clinical and clinical trials. Apply now and join us for a life-changing career!
The position In most of our clinical trials we use an IT-system called Interactive Web Response System (IWRS). Going forward we will work with the IT system Randomized Trial Supply Management (RTSM) to handle allocation of treatments to patients, manage shipments to hospitals around the world and ensure that we get the right data from our trials. The RTSM is set-up for each trial, and right now we operate around 50 live trials. Our new Clinical Trial coordinator will be responsible for setting up the RTSM according to the clinical protocol in coordination with a range of stakeholders to ensure that it delivers what is needed. In this role you might expect to be part of a journey we embarked on recently to implement the new RTSM system that will introduce new technology and possibilities to manage clinical trials even better. Together with experienced colleagues, you will be involved in developing processes in our team that will enable us to work smarter in an informal working environment with a high degree of empowerment. To succeed in the job, you will establish and maintain ongoing collaboration with relevant stakeholders within different functions in Novo Nordisk. Qualifications To succeed in this role your specific background is not relevant, although we expect that you have either a Bachelor or Master’s degree with good results. You could be a recent graduate who is looking to explore career opportunities within the pharmaceutical industry. It would be an advantage if you have: Any knowledge within Supply Chain Management, Engineering or similar Previously worked within the pharmaceutical industry Been involved within QMS, writing deviations/non-conformities and project management Experience with IT systems Previous with stakeholder management experience You communicate effectively and fluent in Danish and English You plan and approach tasks in a structured way and seek simple solutions and see continuous improvement as a natural part of processes. In addition, you are a team player and find motivation when reaching common goals.
About the department
The position is in Supply Chain Setup, a team of 16 dedicated professionals responsible for supply strategies and setting up our supply management system. This includes early phase design of the supply chain for clinical trials, forecasting trial product demand and preparing strategies for packaging and distribution. Clinical Supplies Trial Set-up is a part of Clinical Supplies in CMC Development. We are responsible for the planning, production, packaging, labelling and distribution of products for Novo Nordisk clinical trials worldwide. The department consist of four teams, preparing clinical trials for execution by forecasting product demand, simulating trial supply execution, setting up randomization and trial supply management system, preparing labels and directions for use.
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 Søren Bjørnskov, +45 3075 7083.
Deadline
4 August 2023
Application will be reviewed after the deadline has been reached. 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.
The position In most of our clinical trials we use an IT-system called Interactive Web Response System (IWRS). Going forward we will work with the IT system Randomized Trial Supply Management (RTSM) to handle allocation of treatments to patients, manage shipments to hospitals around the world and ensure that we get the right data from our trials. The RTSM is set-up for each trial, and right now we operate around 50 live trials. Our new Clinical Trial coordinator will be responsible for setting up the RTSM according to the clinical protocol in coordination with a range of stakeholders to ensure that it delivers what is needed. In this role you might expect to be part of a journey we embarked on recently to implement the new RTSM system that will introduce new technology and possibilities to manage clinical trials even better. Together with experienced colleagues, you will be involved in developing processes in our team that will enable us to work smarter in an informal working environment with a high degree of empowerment. To succeed in the job, you will establish and maintain ongoing collaboration with relevant stakeholders within different functions in Novo Nordisk. Qualifications To succeed in this role your specific background is not relevant, although we expect that you have either a Bachelor or Master’s degree with good results. You could be a recent graduate who is looking to explore career opportunities within the pharmaceutical industry. It would be an advantage if you have:
About the department
The position is in Supply Chain Setup, a team of 16 dedicated professionals responsible for supply strategies and setting up our supply management system. This includes early phase design of the supply chain for clinical trials, forecasting trial product demand and preparing strategies for packaging and distribution. Clinical Supplies Trial Set-up is a part of Clinical Supplies in CMC Development. We are responsible for the planning, production, packaging, labelling and distribution of products for Novo Nordisk clinical trials worldwide. The department consist of four teams, preparing clinical trials for execution by forecasting product demand, simulating trial supply execution, setting up randomization and trial supply management system, preparing labels and directions for use.
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 Søren Bjørnskov, +45 3075 7083.
Deadline
4 August 2023
Application will be reviewed after the deadline has been reached. 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.
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Måløv.
Jobbet er oprettet på vores service den 4.7.2023, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- Øvrige
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