Sr. Global Pharmacovigilance Scientist

Role: Senior Global Pharmacovigilance Scientist supporting Belite Bio's clinical pipeline targeting retinal degenerative diseases, including Stargardt disease and dry AMD. Responsibilities: manage (S)AE collection, case assessments, data entry, follow-up communications, and expedited reporting to authorities; develop data outputs and respond to regulatory safety inquiries; lead PV training, reconciliation, and signal detection meetings; ensure compliance with global PV regulations and update procedures accordingly; oversee database setup and contribute to safety-related business development activities. Requirements: BS in life sciences, pharmacy, or related field; 3+ years of pharmacovigilance experience, including case processing, aggregate reporting, and signal detection; proficiency with safety databases (ARGUS preferred); strong knowledge of GVP, GCP, ICH guidelines; management and training skills. HighValue: biologics, Phase 3 clinical trials, regulatory compliance, cross-functional collaboration with clinical and regulatory teams. WorkSetup: not specified.