Your main responsibilities will be: acting as Qualified Person for Pharmacovigilance in Czech republic, managing collection, processing, documentation, reporting of all adverse events reports for all products from clinical trials, post-marketing studies, registries etc.
We require University degree (pharmacist or medical doctor), at least 3 years experience in drug safety (or 5 years experience as medical advisor or CRA) and fluent in English (spoken and written).
Candidate has to have excellent communications and negotiation skills, and also leadership and management skills.
If you are interested in this position please send your CV to struzkova@hays.cz
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