Remote Pharmacovigilance Specialist (EN/ES/FR)

IQVIA Inc

Buenos Aires

Remote

ARS 1,800,000 - 3,600,000

Full time

8 days ago

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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.