🛠 Tech Stack

💼 About This Role

You'll join a growing safety team processing individual case safety reports for clinical trials and post-marketing programs across Latin America. You'll ensure regulatory compliance and timely reporting using Argus Safety Database. This role offers the chance to work remotely across multiple countries.

🎯 What You'll Do

• Process ICSRs according to SOPs and project-specific safety plans
• Triage ICSRs, evaluate data for completeness and regulatory reportability
• Enter data into Argus Safety Database
• Draft case narratives and manage query resolution

📋 Requirements

• 2 years of clinical trial drug safety experience
• Bachelor's degree in Pharmacy, Nursing, Life Science, or equivalent
• Experience with Argus Safety Database and MedDRA
• Professional working proficiency in English