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Pharmacovigilance Specialist Job Description
We are seeking a highly experienced Pharmacovigilance Specialist to join our team at IQVIA Argentina. The ideal candidate will have a strong background in pharmacovigilance and regulatory affairs.
Main Responsibilities:
- Process safety data and information across service lines.
- Collect and track incoming Adverse Events (AEs) and endpoint information.
- Database entry, coding AEs and products, writing narratives, and performing literature-related activities.
- Liaise with functional team members and healthcare professionals to address project-related issues.
Requirements
- Bachelor's degree in life sciences or related field.
- Relevant experience with up to 3 years, including up to 1 year of pharmacovigilance experience is valuable.
- Fluency in English, Spanish, and Italian.