- Remoto
- Tiempo completo
- Tiempo parcial
- Contrato
- Medicina
... Clinical-Regulatory content. Experience translating pharmacovigilance content preferred: SAE/AE (serious and non-serious adverse events), PSURs, SUSARs, ICSRs, DSURs, Risk Management Plans (RMP). Alternatively, experience translating regulatory or clinical documents: medical reports, protocols, synopses, ICF, discharge reports, study reports, ...
España, España