Pharmacovigilance Specialist (Fluent in English + German or French)

IQVIA Argentina; Buenos Aires; Presencial; ARS 6.500.000 - 9.750.000; Jornada completa

Descripción de la vacante

A leading clinical research organization is seeking a Trilingual Clinical Research Associate to review and process safety data. The ideal candidate will be fluent in English, Spanish, and German and will have experience in clinical settings. Responsibilities include performing pharmacovigilance activities and ensuring compliance with regulations. This position offers full flexibility with a 100% remote work model and benefits including flexible work hours and an annual performance bonus.

Servicios

OSDE 310

Annual bonus by performance

Salary adjustments for inflation

21 vacation days

Work flexibility

Formación

• Must have a Bachelor’s degree in Life sciences or related field.
• Fluency in English and German is mandatory.
• Up to 3 years of previous clinical experience required.

Responsabilidades

• Process safety data according to applicable regulations and guidelines.
• Perform pharmacovigilance activities including tracking Adverse Events.
• Ensure compliance with quality and delivery standards.
• Liaise with team members and healthcare professionals.

Conocimientos

Fluency in English

Fluency in Spanish

Fluency in German

Clinical experience

Educación

Bachelor’s degree in Life sciences or related field

Descripción del empleo

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 German.

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 German (mandatory)
• Up to 3 years of previous clinical experience.
• 1 year of pharmacovigilance experience will be highly valued (not mandatory)
  

What we offer to you:

• OSDE 310
• Annual bonus by performance
• Salary adjustments during the year according to inflation rates.
• 21 vacations days
• Work flexibility
• 100% remote role!

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