Pharmacovigilance Specialist (Fluent in English + French)

QHR IQVIA Zagreb d.o.o.

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Buenos Aires, Argentina Mexico City, Mexico Until 9/23/2026 0+ years exp First posted July 25, 2026 Last posted July 25, 2026
Job description

Job Overview

Review, assess, and process safety data and information across service lines, received from various sources. Distribute reports/data to both internal and external third parties following applicable regulations, Standard Operating Procedures (SOPs), and internal guidelines under the guidance and support of senior operation team members. This is a trilingual role requiring fluency in English, Spanish, and French.

Main 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.
     

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)

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

About this role

Summary

Process safety data, perform pharmacovigilance activities, ensure compliance, liaise with healthcare professionals

Job title

pharmacovigilance specialist

Experience level

up to 3 years

Minimum experience

0+ years exp

Industry

healthcare

Location requirements

Based in Buenos Aires or Mexico City, no remote work

Salary

Not specified

Management role

No

Skills & keywords

Required skills

fluency in Englishfluency in Frenchlife sciencesclinical experiencepharmacovigilance

Preferred skills

literature reviewdatabase entryregulatory guidelinesAdverse Events

Specializations

pharmacovigilanceclinical dataregulatory complianceliterature reviewdatabase management
Locations

Structured locations inferred from the posting.

Buenos Aires, Argentina

On-site City

Mexico City, CDMX, Mexico

On-site City