About the role
Process and assess adverse-event reports for a pharmaceutical company.
Process and assess adverse-event reports for a pharmaceutical company. This is a hybrid role based in Ljubljana, Slovenia. The successful candidate will join the clinical team and work closely with senior stakeholders.
Responsibilities
- Process individual case safety reports
- Assess seriousness and causality
- Support signal detection and periodic reports
- Ensure compliance with EU GVP
Requirements
- 2+ years in pharmacovigilance
- Knowledge of EU GVP and MedDRA
- Attention to detail