Experteer Overview In this role you support the handling of SAEs and adverse events in clinical trials and market reports, ensuring accurate data capture in safety systems. You will work within the SRS/FSP team dedicated to a sponsor, contributing to pharmacovigilance processes and regulatory compliance. Your work includes case reviews, narrative drafting, coding of events, and assisting with SAE reconciliation and EudraVigilance registration. The position emphasizes collaboration across project teams, maintaining up-to-date knowledge of safety regulations, and improving established safety routines.Compensaciones / Incentivos
- Support SAE handling in clinical trials and market reports under SOPs and regulatory requirements
- Review cases and draft AE/SAE narratives as needed
- Code adverse events, medical history and concomitant medications
- Assist SAE reconciliation and data handling (DCF)
- Support EudraVigilance registration and related matters




- Participate in project groups and cross-departmental meetings
- Update safety handling templates per SOPs and study needs
- Contribute to developing routines to improve safety work processes
- Stay informed on laws, directives, and guidelines for SAE handling and pharmacovigilanceResponsabilidades
- Bachelor’s degree in life science or nursing or equivalent
- Ability to work in a fast-paced environment with changing priorities
- Understanding of medical terminology and drugs/therapeutic areas
- Basic knowledge of GCP, ICH guidelines, pharmacovigilance legislation, and SOPs
- Ability to work independently and in a matrix team structure
- Excellent written and verbal communication
- Proficiency with word processing; spreadsheets desirableRequisitos principales
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📌 Drug Safety Associate (Barcelona)
🏢 Trial Form Support
📍 Barcelona