Clinical Supplies Coordinator (Temporary)
- Research & Development
- Denmark - Måløv
We are looking for a new colleague in Clinical Supplies Coordination.
Would you like to work in a busy environment with coordination of multiple activities together with a dynamic and dedicated team of colleagues? Can you multitask and are you motivated by the challenge of securing a stable supply chain for clinical trials in new and innovative treatments? If yes, we are looking forward to hearing from you.
About the department
The pipeline of potential new products in Novo Nordisk is continuously growing creating a growing portfolio of clinical trials. Our main and most important task in Clinical Supplies Coordination is to ensure that trial products are available on time and in the right quality and quantity for all clinical trials conducted globally by Novo Nordisk.
In order to meet Novo Nordisk’s ambitious goals within diabetes, haemophilia and other chronic diseases, we are furthermore working with reducing our product waste, to shorten our lead time and optimise the use of resources by means of various LEAN tools.
We are around 50 people in Clinical Supplies Coordination and are located at Novo Nordisk site Måløv. The new candidate will be part of a team of dedicated people working with drug candidates for various treatment groups.
The Job
The job is a temporary position for a duration of 12 months. As Clinical Supplies Coordinator, you will be responsible for the clinical supply chain from contributing to the development of the clinical trial protocols, from a trial supply perspective, and until the product reaches the end user. You will work according to GMP and GCP to ensure that the tight deadlines of the development projects are met.
You will be using project management tools and your main responsibilities are planning and coordination of packaging of clinical trial supplies. You will provide input to our web-based trial supply management system and will be writing trial material manuals. You will conduct training of Clinical Research Associates and study site personnel in trial-specific product handling; hence once or twice yearly you will attend international meetings.
In addition to these trial specific responsibilities, you will take part in projects with focus on optimising our processes.
Qualifications
You hold a university degree in natural sciences, engineering or similar. You have at least 3-5 years of experience from the pharmaceutical industry with clinical trial supplies planning. Alternatively, you have at least 5 years of experience from areas such as drug development or drug manufacturing. Knowledge of GMP/GCP is required.
A significant part of our processes are carried out in various IT systems and it is therefore important that you are able to quickly adapt to such systems.
You are comfortable with taking independent action and manoeuvring in an environment characterised by frequent changes. As Clinical Supplies Coordinator, you are placed in the centre of the clinical supply chain and you need to be robust and a strong communicator. We collaborate with colleagues and partners all over the world; therefore you are fluent in both written and spoken English on a professional level.
We expect you to possess a good sense of humour and to be a team player with a positive attitude to changes and challenges. You have a high level of engagement and flexibility and see continuous improvements as natural part of your job.
In this temporary position, you will be able to further develop your supply chain skills and business understanding, work with many contacts across the organisation, and you will broaden your personal competences and skills.
At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes and change their lives. By working with us you will have the opportunity to do the same in a global business environment.
Contact
For further information, please contact Team Leader Nicolas Omdahl, +45 3079 7114.
Deadline
20 December 2013
- Research & Development
- Denmark - Måløv
We are looking for a new colleague in Clinical Supplies Coordination.
Would you like to work in a busy environment with coordination of multiple activities together with a dynamic and dedicated team of colleagues? Can you multitask and are you motivated by the challenge of securing a stable supply chain for clinical trials in new and innovative treatments? If yes, we are looking forward to hearing from you.
About the department
The pipeline of potential new products in Novo Nordisk is continuously growing creating a growing portfolio of clinical trials. Our main and most important task in Clinical Supplies Coordination is to ensure that trial products are available on time and in the right quality and quantity for all clinical trials conducted globally by Novo Nordisk.
In order to meet Novo Nordisk’s ambitious goals within diabetes, haemophilia and other chronic diseases, we are furthermore working with reducing our product waste, to shorten our lead time and optimise the use of resources by means of various LEAN tools.
We are around 50 people in Clinical Supplies Coordination and are located at Novo Nordisk site Måløv. The new candidate will be part of a team of dedicated people working with drug candidates for various treatment groups.
The Job
The job is a temporary position for a duration of 12 months. As Clinical Supplies Coordinator, you will be responsible for the clinical supply chain from contributing to the development of the clinical trial protocols, from a trial supply perspective, and until the product reaches the end user. You will work according to GMP and GCP to ensure that the tight deadlines of the development projects are met.
You will be using project management tools and your main responsibilities are planning and coordination of packaging of clinical trial supplies. You will provide input to our web-based trial supply management system and will be writing trial material manuals. You will conduct training of Clinical Research Associates and study site personnel in trial-specific product handling; hence once or twice yearly you will attend international meetings.
In addition to these trial specific responsibilities, you will take part in projects with focus on optimising our processes.
Qualifications
You hold a university degree in natural sciences, engineering or similar. You have at least 3-5 years of experience from the pharmaceutical industry with clinical trial supplies planning. Alternatively, you have at least 5 years of experience from areas such as drug development or drug manufacturing. Knowledge of GMP/GCP is required.
A significant part of our processes are carried out in various IT systems and it is therefore important that you are able to quickly adapt to such systems.
You are comfortable with taking independent action and manoeuvring in an environment characterised by frequent changes. As Clinical Supplies Coordinator, you are placed in the centre of the clinical supply chain and you need to be robust and a strong communicator. We collaborate with colleagues and partners all over the world; therefore you are fluent in both written and spoken English on a professional level.
We expect you to possess a good sense of humour and to be a team player with a positive attitude to changes and challenges. You have a high level of engagement and flexibility and see continuous improvements as natural part of your job.
In this temporary position, you will be able to further develop your supply chain skills and business understanding, work with many contacts across the organisation, and you will broaden your personal competences and skills.
At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes and change their lives. By working with us you will have the opportunity to do the same in a global business environment.
Contact
For further information, please contact Team Leader Nicolas Omdahl, +45 3079 7114.
Deadline
20 December 2013