id: NDg3NzQ4MyA3

reference: 4877483

documentId: 4877483

connectionPointId: 7

lastModificationDate: 1536738867510

stillingsbetegnelse:
IWRS Coordinator with IT interest & good stakeholder management skills

jobbeskrivelse:

Are you ambitious and motivated by delivering high quality project management and do you thrive on working independently and with many stakeholders? Do you find it interesting to take on the responsibility for an IT system that is essential for the logistics of our clinical trials? Then take the next step in your life-changing career and join us in Clinical Supplies.

About the department
Clinical Supplies Project Planning (CSPP) is a part of Chemistry, Manufacturing and Control (CMC) Development. As part of Novo Nordisk’s R&D family, CMC Development makes a real difference for patients with chronic diseases across the world. We develop, manufacture and distribute drug candidates for non-clinical and clinical trials which is a complicated journey that requires about 10 years of dedicated work in CMC Development. CMC Development is an ambitious organisation with a strong culture. We always seek to solve problems, have an eye for the entire business and do our best to deliver despite any obstacles along the way.

In Clinical Supplies Project Planning, 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 patients participating in our clinical trials.

The position
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 60 trials. As our new IWRS coordinator, 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.

Our department consists of 3 teams; Project Entry, Supply Strategy and IWRS (IT). The position is in the IWRS team where you will work together with 11 IWRS coordinators.

Among your main tasks is to produce a specification of how the system should be programmed. The actual programming is outsourced; however, you will need to collect input from a large number of stakeholders in order to set-up the system in order to ensure that it delivers what is needed. You will also test that the system works, and you will train the end-users. Depending on business need and qualifications a few travel days per year to different countries could be expected in order to support and train the end-users locally.

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 well as you get the opportunity to drive larger projects together with other colleagues.

Qualifications
There are several ways of entering this job. You can be a M.Sc. or B.Sc. within Pharmaceutical Science, Engineering or similar, you can have a background within clinical trials (data management, trial statistician, monitors, trial management or study nurse) or your background can be within IT, preferably with clinical IT systems.

While experience with clinical IT will be an advantage, we will teach you what you need to know. 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 expect you to be independent, self-driven, ambitious and good at multi-tasking and a team player who likes challenges. You must like to handle many different stakeholders, and you should enjoy striving for perfection and working in a structured way. We expect you to have good communication skills in both Danish and English.

Working at Novo Nordisk
At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.

Contact
For further information, please contact Anders Larsen at +45 3075 2669.

Deadline
30 September 2018.

numberOfPosts: 1

jobCategoriesCodes_0: http://data.europa.eu/esco/isco/C2512

abstractJV_contact_0:
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positionTypeCode: directhire

contractTypeCodes_0: fulltime

Arbejdsgiver Navn: Novo Nordisk A/S

source: DK-STAR