Pharmacovigilance Specialist

Pharmacovigilance Specialist (Fixed-term 6 months) This role is ideal if you're looking to start your career in pharmacovigilance. Experience in the field is not required but will be a plus. The position is a fixed‑term role of 6 months, full‑time (Monday‑Friday), home‑based, and may require working on Argentine national holidays. Job Overview Review, assess and process safety data and information (adverse event reports) across service lines. Receive reports from various sources and distribute data to both internal and external third parties following applicable regulations, SOPs and internal guidelines under the guidance and support of senior operation team members. Essential Functions Prioritize and complete assigned trainings on time. Process safety data according to applicable regulations, guidelines, SOPs and project requirements. Perform pharmacovigilance activities per project requirements, including collecting and tracking incoming adverse events and determining initial/update status of events. Enter data into database. Code adverse events and products, write narratives, and perform literature‑related activities as per internal and project timelines. Meet quality standards and productivity/delivery standards per project requirements. Ensure compliance with all project‑related processes and activities. Create, maintain and track cases as applicable to the project plan. Identify quality problems and bring them to the attention of a senior team member. Demonstrate problem‑solving capabilities. Mentor new team members, if assigned by the manager. Attend project team meetings and provide feedback to the operations manager on challenges, issues, or successes. Ensure 100% compliance with all people practices and processes. Perform other duties as assigned. Qualifications Bachelor’s degree in Life Sciences required; students will also be considered. Advanced English – mandatory. Advanced Portuguese – desirable. 1‑1.5 years of relevant work experience, ideally in a health care or clinical research environment. Working knowledge of applicable safety database – desirable. Knowledge of applicable global, regional, local clinical research regulatory requirements – beginner. Good working knowledge of Microsoft Office and web‑based applications. Strong organizational and time‑management skills. About IQVIA IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence. We accelerate the development and commercialization of innovative medical treatments to improve patient outcomes and population health worldwide. Learn more at #J-18808-Ljbffr