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Aktiválás dátuma: 2024-04-04

Állás bemutatása

Feladatok: Enter reports of drug adverse events from post-marketed or clinical study source to the safety database.Provide medical expertise and judgment throughout the case-handling process with medical review of individual cases.You will handle non-serious and serious cases according to regulatory requirements, process instructions and standard operational procedures.Resolves queries related to pharmacovigilance activities and individual case reports.Adhere to global and local procedural documents.Egészségügyi szakember; Gyógyszerész; Orvos, Szakorvos
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