Top Job | 2024. 06. 25. | Teljes munkaidõ | Budapest | IQVIAResponsibilitiesYou will be performing medical review and clarification of trial-related Adverse Events (AEs) and post-marketing adverse drug reactions (ADRs) including narrative content, queries, coding, expectedness, seriousness, causality, and company summaryComposing, editing, and medically reviewing Analyses
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