6d ago

Pharmacovigilance Regulatory Reporting (Trilingual)

2 Locationsmid
Legal & ComplianceRegulatory
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Quick Summary

Overview

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

Technical Tools
Legal & ComplianceRegulatory

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.

  • 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.

Requirements

~1 min read
  • Bachelor's 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.

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.

Location & Eligibility

Where is the job
Not specified
Location terms not specified
Who can apply
Same as job location

About this job

Posted
6 days ago
Employer
has 2,514 open jobs on Jobera in 76 countries.

Listing Details

Posted
October 9, 2026
First seen
October 10, 2026
Last seen
October 15, 2026

Posting Health

Days active
4
Repost count
0
Trust Level
32%
Scored at
October 15, 2026

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Pharmacovigilance Regulatory Reporting (Trilingual)