Pharmacovigilance Specialist

iqvia· BZL IQVIA RDS Brasil Ltda
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📍 São Paulo, BrazilFull time
Full timeBZL IQVIA RDS Brasil Ltda

About this 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 role requires fluency in English 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.
     

Qualifications

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

Work modality:

  • 100% home-based

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 committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Frequently Asked Questions

Is the salary disclosed for the Pharmacovigilance Specialist position at iqvia?
The salary for this Pharmacovigilance Specialist role at iqvia is not publicly listed. Click "Apply Now" to learn more about the compensation package on their official careers page.
Where is the Pharmacovigilance Specialist position at iqvia located?
This Pharmacovigilance Specialist role at iqvia is based in São Paulo, Brazil. The position is listed as on-site or hybrid. Check the full job description or apply directly to confirm the work arrangement.
Is the Pharmacovigilance Specialist role at iqvia full-time or part-time?
This is listed as a Full time position. It is posted as a Pharmacovigilance Specialist role in the BZL IQVIA RDS Brasil Ltda department at iqvia.
Which team or department does the Pharmacovigilance Specialist at iqvia belong to?
This Pharmacovigilance Specialist position is part of the BZL IQVIA RDS Brasil Ltda department at iqvia. See the full job description for more information about the team structure and responsibilities.
How do I apply for the Pharmacovigilance Specialist position at iqvia?
Click the "Apply Now" button on this page. You will be redirected to iqvia's official application portal hosted on workday where you can submit your application directly.
When was the Pharmacovigilance Specialist job at iqvia posted?
This Pharmacovigilance Specialist position at iqvia was posted on Aug 21, 2026. Apply as soon as possible — early applications are often reviewed first.
Pharmacovigilance Specialist
iqvia
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You'll be redirected to iqvia's official application page on Workday.