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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
About Xebia No deje pasar esta oportunidad, inscríbase rápidamente si su experiencia y habilidades coinciden con lo que se indica en la siguiente descripción. For more than 25 years, our global network of passionate technologists and
We are looking for the very Top Talent.and we would be delighted if you were to join our team! Lea atentamente toda la información sobre esta oportunidad y luego utilice el botón de solicitud de abajo