Remote Trilingual Pharmacovigilance Specialist (EN/ES/IT)

IQVIA; Tandil; Remote; ARS 1,200,000 - 2,000,000; Full time

Benefits offered by this job

OSDE 310

Annual bonus by performance

Inflation-based salary adjustments

21 vacation days

Work flexibility

100% remote role

Job summary

IQVIA is seeking a Pharmacovigilance Data Reviewer to process safety data across service lines and distribute reports to internal teams and external partners. Fluent in English, Spanish, and Italian, you will work remotely with support from senior operations staff.

The role involves collecting and tracking adverse events, coding, writing narratives, and literature-related activities while ensuring adherence to SOPs, regulations, and quality standards.

Qualifications

• Bachelor’s degree in Life sciences or a related field (mandatory).
• Fluency in English and Italian (mandatory); Spanish language proficiency 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 regulations, guidelines, SOPs and project requirements.
• Perform pharmacovigilance activities: collect and track Adverse Events and endpoint information, code AEs and products, write narratives, and literature-related tasks.
• Ensure compliance with quality, productivity and delivery standards per project requirements.
• Liaise with functional teams and healthcare professionals to address project-related issues.

Skills

English

Spanish

Italian

Education

Bachelor's degree in Life sciences or related field

Job description

IQVIA is seeking a Pharmacovigilance Data Reviewer to process safety data across service lines and distribute reports to internal teams and external partners. Fluent in English, Spanish, and Italian, you will work remotely with support from senior operations staff.

The role involves collecting and tracking adverse events, coding, writing narratives, and literature-related activities while ensuring adherence to SOPs, regulations, and quality standards.