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Senior Safety Surveillance Adviser in Global Safety (maternity cover)

Maternity covers in Global Safety as a Senior Safety Surveillance Adviser (Biopharm) and a Safety Surveillance Adviser (GLP-1) are open for hire from July and August 2018 respectively.

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 our new colleague in Global Safety.

About the department
Safety Surveillance GLP-1 and Safety Surveillance Biopharm are departments within Global Safety and are situated in Bagsværd, Denmark. Our group of dedicated and skilled professionals has global responsibility for the surveillance of all safety information for a part of Novo Nordisk’s GLP-1 products that are currently under development and for the Biopharm portfolio covering Haemostasis, Growth disorders and Hormone replacement therapies in development and marketed.

The position
In the positions you will be responsible independently or together with colleagues for the ongoing safety surveillance of one or more of our products. Key responsibilities include analysis of safety data (e.g. potential side effects), medical evaluation of safety information received from sites participating in our clinical trials, or from patients or prescribers using a marketed product. 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 teams of highly skilled, committed and enthusiastic colleagues, but you are also 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 an 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 Ida Carøe Helmark (GLP-1 position) at +45 3075 3696 or Hanne Rasmussen (Biopharm position) at +45 3079 7450.

Deadline
29 April 2018.


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