Pharmacovigilance Specialist With Italian

IQVIA UK

Buenos Aires, Argentina
Process safety data
Collect and track adverse events
Database entry and coding
Review, assess and process Safety data and information across service lines received from various sources

Job Summary

  • Review, assess and process Safety data and information across service lines received from various sources.
  • Perform pharmacovigilance activities including collecting and tracking incoming Adverse Events, database entry, coding, writing narratives, and literature-related activities.
  • Ensure compliance with quality, productivity, and delivery standards per project requirements and liaise with different functional team members.

Matching Summary

Review, assess and process Safety data and information across service lines received from various sources.

Skills & Requirements

Must-have

  • Process safety data
  • Collect and track Adverse Events
  • Database entry and coding
  • Fluency in English and Italian

Nice-to-have

  • Liaise with healthcare professionals
  • Work on national ARG holidays

Key Requirements

  • Bachelor’s degree in Life sciences
  • C1 level fluency in English and Italian
  • Up to 3 years clinical experience
  • 1 year pharmacovigilance experience

Work Rights

Not specified

Tailored Resume

Cover Letter