Processing and documentation of drug safety relevant information.
Tasks & Responsibilities
Collection, plausibility check and documentation of reports about drug risks (adverse drug reactions, pharmaceutical-technical defects) in centralized databases
Correspondence regarding the completion of reports about drug risks
Electronic / conventional transmission of adverse drug reaction reports to competent authorities and B. Braun Melsungen affiliates as directed
Supportive organizational activities in the case of drug safety related measures (such as batch recalls, risk minimization activities)
Data base queries, compilation of statistics, presentations and reports
Requirements
Education as pharmaceutical-/medicinal-/chemical-technical assistant or equivalent training
Experience in handling data with computerized systems
Very good English written and spoken
Diligent and well-organized performance
Communication and teamwork skills
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