Job Description

Embark on an exciting journey as our Global Pharmacovigilance Data Specialist! As a pivotal member of our global pharmacovigilance team, you will analyze and interpret 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 will collaborate closely with both internal and external stakeholders to resolve complex issues, uphold process standardization, and translate critical adverse event reports using your multilingual skills in English and a second language such as Portuguese and/or French.

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 ...