Job Description Embark on an exciting journey as our Global 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 multilingual skills, particularly in English and a second language such as French, German, or Portuguese, will be instrumental in translating critical adverse event reports. You will be responsible for: Performing 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. Providing support in written translation of adverse events reports from different countries. Collaborating with internal and external stakeholders to resolve issues of varying complexity to guarantee process standardization and adherence and ensure compliance with reporting requirements. Supporting simplification and optimization of case management activities to enhance overall effectiveness. Education and other Qualifications: Bachelor’s degree or above in health care or life sciences disciplines (Nurse, Veterinary, Pharmacist, Bacteriologist or Biologist/Microbiologist). English Advanced (C1) proficiency or Intermediate B2 with C1 level in writing and reading. A certificate or diploma verifying this level will be required. Upper Intermediate to Advanced proficiency in one of the following languages is a must: French, German, or Portuguese. A certificate or diploma to confirm their proficiency level. At least one year of laboral experience is required. Clinical and/or Pharmacovigilance-related experience is desired. Current Employees apply HERE Current Contingent Workers apply HERE Employee Status: Project Temps (Fixed Term) Relocation: No relocation VISA Sponsorship: No Travel Requirements: No Travel Required Flexible Work Arrangements: Hybrid Shift: Not Indicated Valid Driving License: No Hazardous Material(s): no Job Posting End Date: 04/7/2025 *A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Requisition ID: R341684 #J-18808-Ljbffr