Pharmacovigilance Specialist With French

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

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.