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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**
- Prioritize and complete assigned training on time to ensure up-to-date knowledge of regulations and guidelines.
- Process safety data according to applicable regulations, guidelines, and project requirements.
- 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.
- Work closely with project management, clinical, data management teams, and healthcare professionals to address project-related issues.
- Bachelor's degree in life sciences or related field required.
- Up to 3 years of relevant experience, including up to 1 year of pharmacovigilance experience, highly valued.
- Proficiency in English is a must.
- Good knowledge of medical terminology and applicable safety databases.