Arbejde IWRS Coordinator - temp. Hovedstaden Novo Nordisk A/S - jobtilbud

GÆLDER
stillingsbetegnelse: IWRS Coordinator - temp.

jobbeskrivelse:
- Research & Development - Denmark - Måløv We are looking for an ambitious and talented person who is ready to take on the responsibility for an IT system that is essential for the logistics of our clinical trials. The job is project management oriented and independent. You must be good at interacting with many different people and be a team player. About the department You will join Clinical Supplies which is a part of the Novo Nordisk Research & Development organisation. We are responsible for the planning, production, packaging, labelling and distribution of products for all 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 Project Planning (CSPP) consists of three teams; Project Entry team, Supply Strategy team and the IWRS team. The job 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 specifically set-up for each trial, and right now we operate IWR systems for around 40 trials. It will be your responsibility to get the IWRS up and running for new trials assigned to you and to maintain it during the whole trial period.Among your main tasks is to produce a specification of how the system should be programmed. The actual programming is outsourced. You will therefore need to collect input from a large number of stakeholders, in order to set-up the system so it delivers what is needed. You will also test that the system works and you will train the end-users, so you can expect a few travel days per 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 supply chain planners as well as with our 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 this experience you can get the opportunity to drive larger projects together with other colleagues. Qualifications There are several ways of entering this job. You can be a (newly educated) M.Sc. 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 with clinical or interactive web-based IT 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. We will also make sure 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 and 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 at +45 3079 0520. Deadline 5 January 2016.

Arbejdsgiver Navn: Novo Nordisk A/S

Arbejdsgiver telefonnummer: 44448888

Arbejdsgiver faxnummer: 44442314

Job kort beskrivelse: Farmaceutarbejde

land: Danmark

region: Hovedstaden

krævede uddannelse: Ikke angivet

Kilde til jobtilbud: AMS, Offentlige arbejdsformidlinger, Danmark

GÆLDER

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