Pharmacovigilance Specialist with French

QPL IQVIA RDS Poland Sp. z o.o.; Buenos Aires; Remote; ARS 1,800,000 - 3,600,000; Full time

Job summary

IQVIA Inc is seeking a Safety Data Processing professional to review, assess, and process safety data from multiple sources. The role supports pharmacovigilance activities, data distribution, and regulatory guidance, with fluency in English, Spanish, and French required.

The position emphasizes adherence to SOPs, quality standards, and collaboration with healthcare professionals. It offers a 100% home-based work modality and opportunities in a global life sciences environment.

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

Pharmacovigilance

English

French

Life sciences

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)

Work modality

Work modality: 100% home-based

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. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.