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IQVIA

Pharmacovigilance Regulatory Reporting, Trilingual

IQVIA

. Submit safety reports to regulatory authorities .

Posted 10/9/2026full-timeRemote • United States, Brazil, ArgentinaJuniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in pharmacovigilance activities, regulatory reporting, and safety data processing while ensuring compliance with applicable regulations and quality standards. Proficient in medical terminology and capable of effective communication in English, Spanish, and Portuguese.

Highest-signal resume keywords
Pharmacovigilance ActivitiesRegulatory ReportingSafety Data ProcessingMedical TerminologyArgus Experience

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Safety Data ProcessingRegulatory ReportingQuality ComplianceData AssessmentCase Tracking
Soft Skills
Strong Organizational SkillsAttention to DetailTeam CollaborationIndependent Work
Tools & Technologies
ArgusSafety Databases
Industry Keywords
Life SciencesSOPsHealthcare ProfessionalsProject RequirementsQuality Standards

About the role

Key responsibilities & impact
  • Submit safety reports to regulatory authorities
  • Review, assess, and process safety data and information from various sources
  • Distribute reports/data to internal and external third parties according to applicable regulations, SOPs, and internal guidelines
  • Process safety data according to regulations, guidelines, SOPs, and project requirements
  • Ensure compliance with quality, productivity, and delivery standards
  • Track cases according to the project plan
  • Identify and report quality problems to senior team members
  • Liaise with functional team members and healthcare professionals on project-related issues
  • Attend project team meetings and provide feedback to the operations manager

Requirements

What you’ll need
  • Bachelor's degree in life sciences
  • Advanced level of English, Spanish and Portuguese
  • 1 year of experience in pharmacovigilance activities (mandatory)
  • Experience specifically in regulatory reporting highly valued
  • Previous experience working with Argus desirable
  • Good knowledge of medical terminology and applicable safety databases
  • Strong organizational skills and attention to detail
  • Ability to work independently and as part of a team

Benefits

Comp & perks
  • 100% home-based work modality