Multilingual Pharmacovigilance Specialist (EN/ES/FR)

IQVIA Inc; Buenos Aires; On-site; ARS 900,000 - 1,300,000; Full time

Job summary

IQVIA in Argentina is seeking a life sciences professional to process safety data and support pharmacovigilance activities across multiple service lines. You will collect, code, and narrate adverse events, while coordinating with cross-functional teams under senior supervision.

The role requires fluency in English and French, with a preference for candidates having up to 3 years of clinical or PV experience. This position emphasizes regulatory compliance and data quality in a global context.

Qualifications

• Bachelor’s degree in Life sciences or a related field (mandatory)
• Fluency in English and French (mandatory) (will be evaluated)
• Up to 3 years of previous clinical experience (desirable)
• 1 year of pharmacovigilance experience will be highly valued (desirable)

Responsibilities

• Process safety data according to applicable regulations, guidelines, SOPs, and project requirements.
• Perform pharmacovigilance activities, including collecting and tracking incoming Adverse Events (AEs) and endpoint information, determining initial/update status of incoming events, database entry, coding AEs and products, writing narratives, and literature-related activities.
• Ensure compliance with quality, productivity, and delivery standards per project requirements.
• Liaise with different functional team members and healthcare professionals to address project-related issues.

Skills

English

French

Education

Bachelor's degree in Life sciences

Job description

IQVIA in Argentina is seeking a life sciences professional to process safety data and support pharmacovigilance activities across multiple service lines. You will collect, code, and narrate adverse events, while coordinating with cross-functional teams under senior supervision.

The role requires fluency in English and French, with a preference for candidates having up to 3 years of clinical or PV experience. This position emphasizes regulatory compliance and data quality in a global context.