ICON Clinical Research is seeking a Pharmacovigilance Reporting Associate (Intelligence) to prepare safety reports for clinical trials and post‑marketing activities. You will operate as a safety reporting intelligence processor or lead, ensuring timely submissions and compliance while aligning with ICON values of people, clients and performance.
The role emphasizes collaboration within multidisciplinary teams, adherence to SOPs, and a focus on process improvement to streamline workflows and add
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📌 Pharmacovigilance Safety Reporting Specialist (Hybrid) (Ciudad de México)
🏢 Icon Clinical Research
📍 Ciudad de México
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