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.