Safety & PV Specialist I

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Safety & PV Specialist I based in Brazil.

• This is an opportunity to support critical pharmacovigilance and safety activities within a global life sciences environment.
• The role focuses on the accurate and timely processing, review, coding, and tracking of Individual Case Safety Reports (ICSRs).
• You will contribute to regulatory reporting, safety database activities, literature screening, and product data management.
• The position combines technical precision, regulatory awareness, and close collaboration with international project teams.
• You will work across clinical trial and post-marketing safety activities while following established SOPs and global guidelines.
• Attention to detail, organization, and sound judgment will be essential to maintaining data quality and patient safety.
• The role offers a remote work environment and exposure to diverse projects within the biopharmaceutical industry.