Are you interested in Clinical Research and IT
- Research & Development
- Denmark - Måløv
Are you interested in Clinical Research and IT?
We presently have a position open as IV/WRS Coordinator, Maternity Cover, with start as soon as possible.
We are looking for an ambitious and talented person who is ready to take on the responsibility for an IT system that we use to manage logistics within drug development. The job is project management oriented, independent and requires some travelling. You must be good at interacting with many different people and be a team player. The position is a maternity cover with start as soon as possible and ending 31. March 2015.
Research & Development, Clinical Supplies Labelling and IT, Måløv, Denmark.
About the department
Clinical Supplies is a part of the Novo Nordisk Research & Development organisation located in Måløv. We are responsible for the planning, production, packaging, labelling and distribution of products for Novo Nordisk clinical trials worldwide. We make sure that the required medication is provided to the patients participating in our clinical trials. Our department, Clinical Supplies Labelling & IT (CSLIT) consists of 3 teams; Labelling & Graphics team, Trial Support team and the IV/WRS team.
The Job
In most of our clinical trials we use an IT-system called Interactive Voice/Web Response System (IV/WRS) 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. An IV/WRS is set-up for each trial, and right now we operate systems for around 50 trials. It will be your responsibility to get the IV/WRS up and running for new trials assigned to you and to maintain it during trial conduct.
Among your main tasks is to produce a specification of how the system should be programmed. The actual programming is outsourced. You need to collect input from a large number of stakeholders. You will also test that the systems work and you will train the end users so there are up to 20 travel days a year to different countries.
You will work closely with many stakeholders in Novo Nordisk worldwide e.g. international trial managers, data managers, statisticians, trial monitors, and clinical supplies coordinators as well as with external suppliers. You will develop your skills within IT, project management, people management and management of our external supplier. You will also obtain knowledge of the drug development process.
As you gather experience – or if you already have project management experience - you can get the opportunity to drive larger projects together with other colleagues.
Qualifications
There are several ways of entering the job. You can be a (newly educated) Ms.C. or B.Sc. within pharmaceutical science, engineering or similar, you can have a background within clinical trials (data management, trial statistician, monitor, trial management or study nurse) or your background can be within IT, preferably clinical IT systems or interactive web response systems.
We will make sure that the tasks at hand are aligned with your degree of experience and your need for development and personal challenges, and that support from more experienced colleagues is available in your development process.
We expect you to be independent, self-driven, ambitious, good at multi-tasking and a team player who likes challenges. You must like to handle many stakeholders with different backgrounds. You should enjoy striving for perfection and working in a structured way.
At Novo Nordisk we create value by putting patients first. Every ten seconds two people are diagnosed with diabetes and close to 366 million people worldwide need us. Working here is not just a way to make a living but a way to make a difference.
Contact
For further information, please contact Mariann Florin Skafte, +45 3079 0520.
Deadline
9 January 2014.
- Research & Development
- Denmark - Måløv
Are you interested in Clinical Research and IT?
We presently have a position open as IV/WRS Coordinator, Maternity Cover, with start as soon as possible.
We are looking for an ambitious and talented person who is ready to take on the responsibility for an IT system that we use to manage logistics within drug development. The job is project management oriented, independent and requires some travelling. You must be good at interacting with many different people and be a team player. The position is a maternity cover with start as soon as possible and ending 31. March 2015.
Research & Development, Clinical Supplies Labelling and IT, Måløv, Denmark.
About the department
Clinical Supplies is a part of the Novo Nordisk Research & Development organisation located in Måløv. We are responsible for the planning, production, packaging, labelling and distribution of products for Novo Nordisk clinical trials worldwide. We make sure that the required medication is provided to the patients participating in our clinical trials. Our department, Clinical Supplies Labelling & IT (CSLIT) consists of 3 teams; Labelling & Graphics team, Trial Support team and the IV/WRS team.
The Job
In most of our clinical trials we use an IT-system called Interactive Voice/Web Response System (IV/WRS) 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. An IV/WRS is set-up for each trial, and right now we operate systems for around 50 trials. It will be your responsibility to get the IV/WRS up and running for new trials assigned to you and to maintain it during trial conduct.
Among your main tasks is to produce a specification of how the system should be programmed. The actual programming is outsourced. You need to collect input from a large number of stakeholders. You will also test that the systems work and you will train the end users so there are up to 20 travel days a year to different countries.
You will work closely with many stakeholders in Novo Nordisk worldwide e.g. international trial managers, data managers, statisticians, trial monitors, and clinical supplies coordinators as well as with external suppliers. You will develop your skills within IT, project management, people management and management of our external supplier. You will also obtain knowledge of the drug development process.
As you gather experience – or if you already have project management experience - you can get the opportunity to drive larger projects together with other colleagues.
Qualifications
There are several ways of entering the job. You can be a (newly educated) Ms.C. or B.Sc. within pharmaceutical science, engineering or similar, you can have a background within clinical trials (data management, trial statistician, monitor, trial management or study nurse) or your background can be within IT, preferably clinical IT systems or interactive web response systems.
We will make sure that the tasks at hand are aligned with your degree of experience and your need for development and personal challenges, and that support from more experienced colleagues is available in your development process.
We expect you to be independent, self-driven, ambitious, good at multi-tasking and a team player who likes challenges. You must like to handle many stakeholders with different backgrounds. You should enjoy striving for perfection and working in a structured way.
At Novo Nordisk we create value by putting patients first. Every ten seconds two people are diagnosed with diabetes and close to 366 million people worldwide need us. Working here is not just a way to make a living but a way to make a difference.
Contact
For further information, please contact Mariann Florin Skafte, +45 3079 0520.
Deadline
9 January 2014.