Pharmacovigilance Specialist with English and Portuguese

IQVIA; Ciudad de México; A distancia; MXN 25,000 - 35,000; Jornada completa

Descripción de la vacante

A leading clinical research provider is seeking a Home-based role to review and process safety data, requiring fluency in English, Spanish, and Portuguese. Key responsibilities include managing pharmacovigilance activities and ensuring compliance with quality standards. Candidates must have a Bachelor's degree in life sciences and at least one year of clinical research experience.

Formación

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

Responsabilidades

• Process safety data according to applicable regulations.
• Perform pharmacovigilance activities including managing Adverse Events.
• Ensure compliance with quality and productivity standards.
• Liaise with team members and healthcare professionals.
• Mentor new team members and support department initiatives.

Conocimientos

Fluency in English

Fluency in Spanish

Fluency in Portuguese

Reporting skills

Clinical research experience

Educación

Bachelor’s degree in life sciences or related field

Descripción del empleo

Home-based role

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 or final year)

• Advanced level of English and Portuguese (mandatory, will be evaluated)

• 1+ year of previous experience in clinical research.

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 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.

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