Multilingual Pharmacovigilance Specialist (EN/DE/ES)

IQVIA; Buenos Aires; Presencial; ARS 700.000 - 1.100.000; Jornada completa

Descripción de la vacante

IQVIA in Argentina is seeking a pharmacovigilance professional with a Life sciences background to review, process, and report safety data from multiple sources. The role requires fluency in English, Spanish, and German and involves PCA activities, data entry, literature work, and stakeholder liaison to ensure quality and timely delivery.

The position emphasizes adherence to SOPs and regulatory guidelines, with collaboration across teams and with healthcare professionals to resolve

Formación

• Bachelor’s degree in Life sciences or a related field (mandatory)
• Fluency in English and German (mandatory) (will be evaluated)
• Up to 3 years of previous clinical experience (desirable)
• 1 year of pharmacovigilance experience will be highly valued (desirable)

Responsabilidades

• 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.

Conocimientos

Fluency in English

Fluency in German

Educación

Bachelor’s degree in Life sciences or related field

Descripción del empleo

IQVIA in Argentina is seeking a pharmacovigilance professional with a Life sciences background to review, process, and report safety data from multiple sources. The role requires fluency in English, Spanish, and German and involves PCA activities, data entry, literature work, and stakeholder liaison to ensure quality and timely delivery.

The position emphasizes adherence to SOPs and regulatory guidelines, with collaboration across teams and with healthcare professionals to resolve