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Position Overview This role leads the technical writing, dossier compilation, and procedural management for genetically modified (GM) crops and gene-edited products (New Breeding Techniques - NBTs) in Brazil. The Lead will combine a process-driven mindset with
What the Associate II, Pharmacovigilance does at Worldwide Responsible for the collection, processing, evaluation and reporting of incoming Serious Adverse Event (SAE) data according to applicable regulatory guidelines/requirements, Worldwide Standard Operating Procedures (SOPs) and project specific
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