Pharmacovigilance analyst
ColombiaMichael Page Colombia
...of information reported from clinical trials, post‑marketing studies, and spontaneous adverse events for marketed products and devices. * Complete case follow‑up as directed or required. * Be responsible for generating and submitting the necessary case reports required for expedited reporting to the MoH/RA. * Reconcile case [...]
Hace 2 días en MichaelPage