Job Search and Career Advice Platform

¡Activa las notificaciones laborales por email!

Pharmacovigilance Specialist with English and Portuguese

IQVIA

Ciudad de México

Presencial

MXN 200,000 - 400,000

Jornada completa

Ayer
Sé de los primeros/as/es en solicitar esta vacante

Genera un currículum adaptado en cuestión de minutos

Consigue la entrevista y gana más. Más información

Descripción de la vacante

A leading healthcare technology company in Mexico City is seeking a candidate for a trilingual role. Responsibilities include processing safety data and performing pharmacovigilance activities. The ideal candidate should have a Bachelor’s in life sciences and at least 1 year of clinical research experience with fluency in English, Spanish, and Portuguese.

Formación

  • 1+ year of previous experience in clinical research.
  • Advanced level of English and Portuguese mandatory.

Responsabilidades

  • Process safety data according to applicable regulations and guidelines.
  • Perform pharmacovigilance activities including tracking incoming events.
  • Mentor new team members and support department initiatives.

Conocimientos

Fluent in English
Fluent in Spanish
Fluent in Portuguese

Educación

Bachelor’s degree in life sciences or a 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 Portuguese.

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.
  • Mentor new team members and support department initiatives as assigned by the manager.
Qualifications
  • Bachelor’s degree in life sciences or a related field. (Graduated)
  • Advanced level of English and Portuguese (mandatory, will be evaluated)
  • 1+ year of previous experience in clinical research.
Consigue la evaluación confidencial y gratuita de tu currículum.
o arrastra un archivo en formato PDF, DOC, DOCX, ODT o PAGES de hasta 5 MB.