IRT Coordinator
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Are you interested in having the daily oversight & responsibility of one of the backbone systems in Novo Nordisk clinical trials globally? Are you eager to learn how Novo Nordisk develops and run clinical trials? If yes, then we have the perfect opportunity for you! Apply now! The Position
In most of our clinical trials we use the IT systems (Interactive Response Technology - IRTs) called RTSM (Randomisation and Trial Supplies Management) or IWRS (Interactive Web Response System) to handle allocation of treatments to patients, manage shipments to clinical sites worldwide and ensure that we get the right data from our trials. The IRTs are set-up for each trial, and right now we operate RTSM/IWRS for estimated 60 trials.
As our new IRT Coordinator, you will be responsible for the daily support of each of these individually build trials in the RTSM/IWRS, e.g.: Supporting in case of escalated cases with our vendor Implementing, testing and documenting updates to ongoing trials Supporting and training to users in the system and much more
Qualifications
We would like to see these qualifications in the ideal candidate: Bachelor’s or master’s degree within engineering, pharmaceutical science, business development or similar Experience from the pharmaceutical industry and IT systems, and an understanding of the GCP/GMP environment Fluency in Danish and English MS Office skills We are looking for someone who can plan and approach tasks in a structured way and seek simple solutions and see continuous improvement as a natural part of processes. As a person, you are detail oriented and at the same time able to see the big picture. It is crucial to be a team player and find motivation when reaching common goals. You like juggling with several issues at a time and enjoy solving these in close collaboration with various internal and external stakeholders.
About the department
The position is in Trial Product Handling; a team of 14 dedicated colleagues responsible for maintaining IRT systems for all trials, handling temperature deviations in clinical trials, quality/training support and general trial product handling support to affiliates at clinical sites globally.
As part of Novo Nordisk’s R&D family, CMC Development & Scaling 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.
Supply Chain Planning is a part of Clinical Supplies in CMC Development & Scaling. 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/monitoring product demand, ordering products/materials, planning the packaging/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
Novo Nordisk is its people. We know that life is anything but linear and balancing what is important at different stages of our career is never easy. That’s why we make room for diverse life situations, always putting people first. We value our employees for the unique skills they bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk is working toward something bigger than ourselves, and it’s a collective effort. Novo Nordisk relies on the joint potential and collaboration of its more than 40,000 employees. Together, we go further. Together, we’re life changing.
Contact
For further information, please contact Katrine Elkjær Mønsted, +4530756956
Deadline
7 October 2023
Please note that applications will be reviewed on an ongoing basis and interviews will be scheduled as soon as suitable candidates are identified.
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.
In most of our clinical trials we use the IT systems (Interactive Response Technology - IRTs) called RTSM (Randomisation and Trial Supplies Management) or IWRS (Interactive Web Response System) to handle allocation of treatments to patients, manage shipments to clinical sites worldwide and ensure that we get the right data from our trials. The IRTs are set-up for each trial, and right now we operate RTSM/IWRS for estimated 60 trials.
As our new IRT Coordinator, you will be responsible for the daily support of each of these individually build trials in the RTSM/IWRS, e.g.:
Qualifications
We would like to see these qualifications in the ideal candidate:
About the department
The position is in Trial Product Handling; a team of 14 dedicated colleagues responsible for maintaining IRT systems for all trials, handling temperature deviations in clinical trials, quality/training support and general trial product handling support to affiliates at clinical sites globally.
As part of Novo Nordisk’s R&D family, CMC Development & Scaling 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.
Supply Chain Planning is a part of Clinical Supplies in CMC Development & Scaling. 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/monitoring product demand, ordering products/materials, planning the packaging/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
Novo Nordisk is its people. We know that life is anything but linear and balancing what is important at different stages of our career is never easy. That’s why we make room for diverse life situations, always putting people first. We value our employees for the unique skills they bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk is working toward something bigger than ourselves, and it’s a collective effort. Novo Nordisk relies on the joint potential and collaboration of its more than 40,000 employees. Together, we go further. Together, we’re life changing.
Contact
For further information, please contact Katrine Elkjær Mønsted, +4530756956
Deadline
7 October 2023
Please note that applications will be reviewed on an ongoing basis and interviews will be scheduled as soon as suitable candidates are identified.
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 "Supply Chain Management", og befinder sig i kategorien "Ledelse og personale".
Arbejdsstedet er beliggende i Måløv.
Jobbet er oprettet på vores service den 20.9.2023, 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.
- Supply Chain Management
- Måløv
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