License Compliance & Revenue Forecasting Lead

PwC; Buenos Aires; Remote; ARS 68,155,000 - 98,446,000; Full time

Job summary

IQVIA in LatAm is seeking a Regulatory Reporting Specialist (Pharmacovigilance) to support submissions to regulatory authorities. The role spans data processing, compliance with SOPs, and cross‑functional collaboration across teams in Brazil and Argentina. Fluency in English, Spanish and Portuguese is required, with home-based work options.

The position emphasizes accuracy, timely case tracking, and teamwork with the operations and regulatory teams to ensure safe and compliant reporting.

Qualifications

• Bachelor's degree in life sciences.
• Languages: advanced English, Spanish and Portuguese.
• 1 year of pharmacovigilance experience (mandatory).
• Experience with Argus is desirable.
• Good knowledge of medical terminology and safety databases.

Responsibilities

• Process safety data according to regulations and SOPs.
• Ensure quality, productivity and timely delivery per project requirements.
• Track cases within the project plan.
• Identify and report quality problems to senior team members.
• Liaise with cross-functional teams and healthcare professionals to address issues.
• Attend project meetings and provide feedback to operations management.

Skills

Pharmacovigilance

English

Spanish

Portuguese

ARGUS

Education

Life sciences degree

Tools

Argus

Job description

IQVIA in LatAm is seeking a Regulatory Reporting Specialist (Pharmacovigilance) to support submissions to regulatory authorities. The role spans data processing, compliance with SOPs, and cross‑functional collaboration across teams in Brazil and Argentina. Fluency in English, Spanish and Portuguese is required, with home-based work options.

The position emphasizes accuracy, timely case tracking, and teamwork with the operations and regulatory teams to ensure safe and compliant reporting.