Embark on an exciting journey as our Integral Pharmacovigilance Data Specialist

As a pivotal member of our global pharmacovigilance team, you'll shine in the analysis and interpretation of intricate adverse event reports from a multitude of sources and therapeutic areas. Your expertise will be crucial in ensuring our investigational and marketed products meet stringent safety standards. In this dynamic role, you'll collaborate closely with both internal and external stakeholders to resolve complex issues and uphold process standardization. Your bilingual skills in English will be instrumental in translating critical adverse event reports.

Responsibilities

• Perform analysis, interpretation, and data entry of adverse event reports from a wide range of sources and therapeutic areas, demonstrating increasing proficiency in clinical knowledge, processes, and regulatory guidelines.
• Provide support in written translation of adverse events reports fr...