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Job Overview This role involves reviewing and processing safety data, ensuring compliance with regulations, SOPs, and project requirements. You’ll be part of a team focused on pharmacovigilance activities, specifically for regulatory reporting and submission to ANVISA. Key Responsibilities Complete assigned trainings on time. Process safety data following regulations, guidelines, and SOPs. Perform pharmacovigilance activities, including collecting and tracking Adverse Events (AE), database entry, coding AE and products, and writing narratives. Ensure quality and productivity standards are met. Liaise with team members and healthcare professionals to address project-related issues. Mentor new team members if assigned. Attend project team meetings and provide feedback. Lead/Support department initiatives. Maintain 100% compliance towards all practices and processes. Qualifications Bachelor’s degree in life sciences or related field with up to 3 years of relevant experience, including at least 1 year of Pharmacovigilance experience. Advanced level of English. Proficiency in Spanish is good to have. Good knowledge of medical terminology and applicable safety databases. Excellent attention to detail, organizational skills, and communication skills. Ability to multi-task, meet deadlines, and adapt to changing demands. Willingness to learn new skills and work as a team player. #LI-REMOTE IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world.
