IWRS Coordinator
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Måløv
- Clinical Development and Medical
- Måløv
Do you have a desire to take on the responsibility for setting up an IT system that is essential for the logistics of our clinical trials? Are you eager to learn about Clinical Research? If Yes, then we have the perfect opportunity for you!
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.
About the department
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.
The position
The position is in Supply Chain Setup, a team of 12 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.
In most of our clinical trials we use an IT-system called Interactive Web Response System (IWRS) 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 IWRS is set-up for each trial, and right now we operate IWRS for around 50 trials. As our new IWRS coordinator, you will be responsible for setting up the IWRS according to the clinical protocol in coordination with a range of stakeholder to ensure that it delivers what is needed.
You will also be part of a journey we embarked on recently to implement a new IWRS system that will introduce new technology and possibilities to manage clinical trials even better.
Qualifications
You hold a Bachelor’s or Master’s degree within Supply Chain Management, Engineering or similar. You have relevant experience within Supply Chain Management, Clinical Supplies, IT or is a talented recent graduate. Experience from the pharmaceutical industry is an advantage. You plan and approach tasks in a structured way and seek simple solutions and see continuous improvement as a natural part of processes. You are a team player and find motivation when reaching common goals. You communicate effectively and fluent in Danish and English.
Working at Novo Nordisk
At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.
Contact
For further information, please contact Søren Bjørnskov, +45 3075 7083.
Deadline
15 January 2020.
Millions rely on us
To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronical diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.
Information og data
Denne ledige stilling har jobtypen "Projektleder", og befinder sig i kategorien "Ledelse og personale".
Arbejdsstedet er beliggende i Måløv.
Jobbet er oprettet på vores service den 16.12.2019, 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.
- Projektleder
- Måløv
- Onsdag den 15. januar 2020
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