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Scope and aim of the post
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