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Safety Operations Adviser


Tööpakkumine on aegunud!

Tööpakkumise number 35033

Tööpakkumise number


Job Description


Ensure appropriate medical interpretation and evaluation of adverse events reported from world-wide sources, from clinical trials and from marketed use.

Ensure the fulfilment of global regulatory requirements to the collection, evaluation and reporting of safety information on all company’s products, i.e. spontaneously reported adverse events, serious adverse events from clinical trials, investigator sponsored trials, named patients supplies and third party trials.

Maintain a network of safety contacts


Medical Doctor, Master Degree in Pharmacy or equivalent
Documented scientific experience, preferably from the pharmaceutical industry
Preferably documented experience with evaluation of drug safety, including a good knowledge of international legal requirements for drug safety vigilance and reporting.
A good knowledge of clinical development
An extremely good knowledge of diseases, their clinical manifestations, treatment and complications.
A good knowledge of clinical pharmacology
A good knowledge of computers and databases
Fluent English, both written and spoken.

Company offers

Competitive salaries based on experience level and relocation packages will be offered.

Additional information

Job location: Denmark

Foreign country
Job type:
full-time, employee
Expiration date:
10. oktoober 2004
16. september 2004


Out partner from Denmark is specialised in recruitment of scientific staff. All their consultants offer the unique combination of a science background combined with recruitment expertise and experience.

One of the customers, a Danish multinational pharmaceutical company located in Copenhagen is looking for a Safety Operations Adviser for their International Product Safety division