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Adverse Event Processor

hace 1 semana


Buenos Aires, Buenos Aires C.F., Argentina IQVIA A tiempo completo
Job Summary
We are seeking a skilled Safety Data Specialist to join our team at IQVIA. In this role, you will play a critical part in ensuring the quality and accuracy of safety data. If you have a strong background in pharmacovigilance and excellent analytical skills, we encourage you to apply.

**Responsibilities and Qualifications**
  1. Prioritize and complete assigned training on time to ensure up-to-date knowledge of regulations and guidelines.
  2. Process safety data according to applicable regulations, guidelines, and project requirements.
  3. Perform pharmacovigilance activities, including collecting and tracking adverse events (AEs), determining event status, database entry, coding AEs and products, writing narratives, and literature-related activities.
  4. Work closely with project management, clinical, data management teams, and healthcare professionals to address project-related issues.
  5. Bachelor's degree in life sciences or related field required.
  6. Up to 3 years of relevant experience, including up to 1 year of pharmacovigilance experience, highly valued.
  7. Proficiency in English is a must.
  8. Good knowledge of medical terminology and applicable safety databases.