Global Pharmacovigilance Data Specialist – Trilingual

About the role

Join our global pharmacovigilance team as a Data Specialist, where you will analyse and interpret complex adverse event reports across multiple therapeutic areas. Your trilingual abilities in English, Portuguese and/or French will be essential for translating critical safety information and ensuring compliance with stringent regulatory standards.

Key responsibilities

• Perform analysis, interpretation and data entry of adverse event reports from diverse sources and therapeutic areas.
• Translate adverse event reports from Portuguese and/or French into English, maintaining accurate clinical terminology.
• Collaborate with internal and external stakeholders to resolve complex safety issues and uphold process standardisation.
• Support simplification and optimisation of case‑management activities to improve overall effectiveness.
• Ensure compliance with regulatory reporting requirements and safety standards.

Required profile

• Bachelor’s degree or higher in a health‑care or life‑science discipline (e.g., nursing, veterinary, pharmacy, microbiology).
• Advanced English proficiency (C1) with certified documentation.
• Upper‑intermediate to advanced proficiency in Portuguese and/or French, with certification.
• Minimum one year of relevant clinical or pharmacovigilance experience.

Required skills

• Bacteriology
• Case Management
• Clinical Data Cleaning
• Clinical Data Management
• Data Analysis
• Database Development
• Data Processing
• Data Quality Assurance
• Data Review
• Data Validation
• Data Visualization
• Electronic Data Capture (EDC)
• Microbiological Cultures
• Microbiology
• Pharmacovigilance
• PL/SQL
• Process Standardization
• Regulatory Compliance
• Safety Standards