Clinical Trials Supply Manager
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Hørsholm
The position
Due to a high level of activity in ALK, we are looking for a skilled Clinical Trial Supply Manager. You will be a part of a small and dedicated team of three people, who support across the global organisation.
The Clinical Trial Supplies team is part of Global Clinical Development. In Global Clinical Development, we are responsible for managing clinical drug development worldwide from early development phases to product introduction. They ensure documentation for clinical submissions and authorities while ensuring that the process lives up to global standards, regulations and business ethics.
Fields of responsibility
As Clinical Trial Supply Manager, you will be an important member of the Clinical Supplies team with the overall responsibility for the provision of clinical trial materials from forecasting and sourcing to distribution. This includes IMP, rescue medication, and diagnostics to be labelled, packaged and distributed according to GxP requirements and the trial protocol specifications as well as planning, set-up and maintenance of IWR solutions. You will be joining one or more clinical trial teams, where you will have the responsibility for all aspects of the timely delivery of clinical trials supplies.
In this position, you will take an important part in supporting the clinical studies across the company, coordinating and delivering supplies throughout the entire value chain, where you will ensure ordering the right amounts of IMP. We collaborate with several teams in ALK, CMOs and CROs to succeed with this.
It will be your responsibility to give input to the trial protocols. This position will also give you a high level of visibility, as you will collaborate with many stakeholders across and outside Global Clinical Development.
Your qualifications
We offer
ALK provides a dynamic and pleasant work environment, complete with inspiring and challenging assignments. The results of your efforts will be significant throughout the organization and you will be able to actively influence and challenge the status quo. Our flat structures attract independent individuals who like to feel the progress of the business and enjoy being close to the decision-making process. You will be part of an engaged and informal team who values skill and knowledge creation. We consider our pioneering spirit coupled with our trustworthiness our winning formula. ALK is a health focused organization and our offices offer a green view of the DTU Science Park in Hørsholm.
Application deadline
The application deadline is January 13th, 2020.
Contact
For further information on the position please contact Senior Director David Mollerup, +45 6191 1081.
Due to a high level of activity in ALK, we are looking for a skilled Clinical Trial Supply Manager. You will be a part of a small and dedicated team of three people, who support across the global organisation.
The Clinical Trial Supplies team is part of Global Clinical Development. In Global Clinical Development, we are responsible for managing clinical drug development worldwide from early development phases to product introduction. They ensure documentation for clinical submissions and authorities while ensuring that the process lives up to global standards, regulations and business ethics.
Fields of responsibility
As Clinical Trial Supply Manager, you will be an important member of the Clinical Supplies team with the overall responsibility for the provision of clinical trial materials from forecasting and sourcing to distribution. This includes IMP, rescue medication, and diagnostics to be labelled, packaged and distributed according to GxP requirements and the trial protocol specifications as well as planning, set-up and maintenance of IWR solutions. You will be joining one or more clinical trial teams, where you will have the responsibility for all aspects of the timely delivery of clinical trials supplies.
In this position, you will take an important part in supporting the clinical studies across the company, coordinating and delivering supplies throughout the entire value chain, where you will ensure ordering the right amounts of IMP. We collaborate with several teams in ALK, CMOs and CROs to succeed with this.
It will be your responsibility to give input to the trial protocols. This position will also give you a high level of visibility, as you will collaborate with many stakeholders across and outside Global Clinical Development.
Your qualifications
- M.Sc. in Pharmacy or similar
- 2-4 years of experience with clinical trial supply coordination
- Experience with CMO collaborations
- Knowledge of GMP and GCP
- Strong planning and communication skills
- Ability to work independently in a varied and complex job
- Service-minded and fluently in spoken and written English
We offer
ALK provides a dynamic and pleasant work environment, complete with inspiring and challenging assignments. The results of your efforts will be significant throughout the organization and you will be able to actively influence and challenge the status quo. Our flat structures attract independent individuals who like to feel the progress of the business and enjoy being close to the decision-making process. You will be part of an engaged and informal team who values skill and knowledge creation. We consider our pioneering spirit coupled with our trustworthiness our winning formula. ALK is a health focused organization and our offices offer a green view of the DTU Science Park in Hørsholm.
Application deadline
The application deadline is January 13th, 2020.
Contact
For further information on the position please contact Senior Director David Mollerup, +45 6191 1081.
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Hørsholm.
Jobbet er oprettet på vores service den 19.12.2019, 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.
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