Top Job | 2025. 04. 30. | Teljes munkaidõ | Budapest | IQVIAResponsibilities You 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 summary Composing, editing, and medically reviewing
Nézze később