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Pharmacovigilance Regulatory Reporting (Trilingual)

IQVIA


Job Location:

São Paulo - Brazil

Monthly Salary: Not provided by the employer
Posted: 30 July 2026 (30+ days ago)
Application Deadline: 27 October 2026
Vacancies: 1 Vacancy

Job Summary

As a Regulatory Reporting Specialist you will be involved in submitting safety reports to regulatory authorities.

Review assess and process safety data and information received from various sources. Distribute reports/data to 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.

Essential Functions

  • Process safety data according to applicable regulations guidelines SOPs and project requirements.
  • Ensure compliance with quality productivity and delivery standards per project requirements.
  • Track cases as applicable to the project plan.
  • Identify and report quality problems to senior team members.
  • Liaise with different functional team members and health care professionals to address project-related issues.
  • Attend project team meetings and provide feedback to the operations manager on challenges issues or successes.

Qualifications

  • Bachelors degree in life sciences
  • Languages: Advanced level of English Spanish and Portuguese.
  • 1 year of experience in pharmacovigilance activities (mandatory) Specifically in regulatory reporting will be highly valued.
  • Previous experience working with Argus is desirable.
  • Good knowledge of medical terminology and applicable safety databases.
  • Strong organizational skills attention to detail and ability to work independently and as part of a team.

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

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.


About Company

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IQVIA is the Human Data Science Company™. We are inspired by the industry we serve and provide solutions that enable life sciences companies to innovate with confidence, maximize opportunities and ultimately drive human health outcomes forward. Our approach is Human Data Science – a d ... View more

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