Pharmacovigilance Specialist with English and Portuguese advanced

hace 3 días


Municipio de Esquel, Argentina IQVIA A tiempo completo

Pharmacovigilance Specialist with English and Portuguese advanced (Fixed-term, 6 months) Fixed-term role for 6 months English and Portuguese advanced mandatory (C1 level in both languages) Full-time position, Monday to Friday Work modality: Home-based May require working on Argentine national holidays Job Overview Review, assess and process Safety data and information (adverse event reports) across service lines, received from various sources and distribute reports/data onward 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 requirement including but not limited to collecting and tracking incoming Adverse Events (AE)/endpoint information. Determine initial/update status of incoming events. Database entry. Coding AE and products, writing narratives, literature-related activities as per internal/project timelines. Ensure compliance to quality standards per project requirements. Ensure compliance to productivity and delivery standards per project requirements. Ensure compliance to all project-related processes and activities. Create, maintain and track cases as applicable to the project plan. Identify quality problems, if any, 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 operations manager on any challenges/issues or successes. Maintain 100% compliance towards all people practices and processes. Perform other duties as assigned. Qualifications Bachelor’s degree in Life Sciences required; students will be considered as well. English and Portuguese advanced. 1-1.5 years of relevant work experience, ideally in 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 skills and time management skills. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at Seniority level Entry level Employment type Full-time Job function Management and Manufacturing Industries Hospitals and Health Care #J-18808-Ljbffr



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