Arbejde Senior Safety Surveillance Advisers in Global Safety (maternity cover) unspecified NOVO NORDISK A/S - jobtilbud

GÆLDER
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reference: 4873958

documentId: 4873958

connectionPointId: 7

lastModificationDate: 1536132272170

stillingsbetegnelse:
Senior Safety Surveillance Advisers in Global Safety (maternity cover)

jobbeskrivelse:

Would you like to be part of an organisation of highly talented pharmacovigilance professionals? Are you naturally curious and analytical? Do you want to play a key role in ensuring highest safety and lowest possible risk to patients that use Novo Nordisk products? Then you may be one of our new colleagues in Global Safety. The positions are open for planned hire 01 November 2018 with a contract period of 14-18 months.

About the department
Safety Surveillance is a department within Global Safety and is situated in Bagsværd, Denmark. Our group of dedicated and skilled professionals has global responsibility for the surveillance of all safety information for Novo Nordisk’s products that are currently under development.

The position
You will be responsible together with other colleagues for the ongoing safety surveillance of one of our products within Semaglutide or Obesity. Key responsibilities include analysis of aggregated safety data, medical evaluation of safety information received from sites participating in our clinical trials, or from patients or prescribers. A core activity is signal detection and the management hereof. You will also provide input to the collection and handling of safety information for new trials and upon completion of a trial give input to the clinical trial report.

You will work in collaboration with a team of highly skilled, committed and enthusiastic colleagues, but you should also be able to work independently. Assuming responsibility, communicating information and taking action will be a part of your work day.

Qualifications
You have a university degree within Natural Sciences (MD, DVM, M.Sc. Pharm. or equivalent). A good understanding of medical concepts, disease processes and scientific methodology is important and experience within drug development and or Pharmacovigilance is a clear advantage.

As you have an analytical, curious mind and possess a quality mind-set, you naturally strive for excellence and meet agreed deliverables. You are service oriented and flexible, which makes you a good team player. You are responsible and take ownership of your tasks, adapt to changes quickly and will constantly look for improvement opportunities.

You must be fluent in English, both written and spoken and be an experienced user of MS Office (Excel, PowerPoint, Word and Outlook).

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 Poul-Martin Haahr at +45 3075 4082 or Ida Carøe Helmark at +45 3075 3696.

Deadline
16 September 2018.



numberOfPosts: 1

jobCategoriesCodes_0: http://data.europa.eu/esco/isco/C2131

abstractJV_contact_0:
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positionTypeCode: directhire

contractTypeCodes_0: fulltime

Arbejdsgiver Navn: NOVO NORDISK A/S

source: DK-STAR

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