Pharmacovigilance Regulatory Reporting Specialist

Location: 100% home-based in São Paulo, Brazil

Company

IQVIA provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

• Process and submit safety data and regulatory reports according to applicable regulations, SOPs, guidelines, and project requirements.
• Review, assess, and distribute safety reports and data to internal and external stakeholders.
• Track cases against project plans and maintain quality, productivity, and delivery standards.
• Identify and report quality issues to senior operations team members.
• Collaborate with functional teams and healthcare professionals to resolve project-related issues.
• Participate in project meetings and provide feedback on challenges, issues, and successes.

Requirements

• Bachelor's degree in life sciences.
• Advanced English.
• 2–3 years of pharmacovigilance experience, with regulatory reporting experience highly valued.
• Previous experience using Argus.
• Knowledge of medical terminology and applicable safety databases.
• Strong organization, attention to detail, and ability to work independently and collaboratively.

Culture & Benefits

• 100% home-based work modality.
• Work within a global life sciences and healthcare intelligence organization.
• Collaboration with cross-functional teams and healthcare professionals.
• Employment focused on regulated safety reporting and patient outcomes.