Job Description

Responsibilities:

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

Requirements

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.