Pharmacovigilance Specialist (Fluent in English + German or French)
Posted by IQVIA • June 09, 2026
Description
Review, assess, and process safety data and information across service lines, received from various sources. Distribute reports/data to both internal and external third parties following applicable regulations, Standard Operating Procedures (SOPs), and internal guidelines under the guidance and support of senior operation team members. This is a trilingual role requiring fluency in English, Spanish, and German (or) French.
Main Responsibilities
Process safety data according to applicable regulations, guidelines, SOPs, and project requirements.
Perform pharmacovigilance activities, including collecting and tracking incoming Adverse Events (AEs) and endpoint information, determining initial/update status of incoming events, database entry, coding AEs and products, writing narratives, and literature-related activities.
Ensure compliance with quality, productivity, and delivery standards per project requirements.
Ready to Seal the Deal?
Submit your application today and take the next step in your career with IQVIA.
Apply for this Job