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1,000 vagas de computer em Brasil. Encontre vagas atualizadas diariamente.
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Associate II, Pharmacovigilance
Há 12 horas
Eldorado do Sul, Rio Grande do Sul, Brasil Worldwide Clinical Trials Tempo integralWhat 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 instructions. Serves as Lead PV Associate on moderate to...
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Associate II, Pharmacovigilance
Há 12 horas
Sapiranga, Rio Grande do Sul, Brasil Worldwide Clinical Trials Tempo integralWhat 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 instructions. Serves as Lead PV Associate on moderate to...
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Associate II, Pharmacovigilance
Há 12 horas
Mogi Guaçu, State of São Paulo, Brasil Worldwide Clinical Trials Tempo integralWhat 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 instructions. Serves as Lead PV Associate on moderate to...
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Associate II, Pharmacovigilance
Há 12 horas
Rio Grande, State of Rio Grande do Sul, Brasil Worldwide Clinical Trials Tempo integralWhat 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 instructions. Serves as Lead PV Associate on moderate to...
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Associate II, Pharmacovigilance
Há 12 horas
Porto Velho, State of Rondônia, Brasil Worldwide Clinical Trials Tempo integralWhat 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 instructions. Serves as Lead PV Associate on moderate to...
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Associate II, Pharmacovigilance
Há 1 dia
Novo Hamburgo, Rio Grande do Sul, Brasil Worldwide Clinical Trials Tempo integralWhat 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 instructions. Serves as Lead PV Associate on moderate to...
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Associate II, Pharmacovigilance
Há 1 dia
Macaé, Rio de Janeiro, Brasil Worldwide Clinical Trials Tempo integralWhat 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 instructions. Serves as Lead PV Associate on moderate to...
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Associate II, Pharmacovigilance
Há 1 dia
Tijucas, Santa Catarina, Brasil Worldwide Clinical Trials Tempo integralWhat 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 instructions. Serves as Lead PV Associate on moderate to...
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Associate II, Pharmacovigilance
Há 1 dia
Campo Largo, Paraná, Brasil Worldwide Clinical Trials Tempo integralWhat 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 instructions. Serves as Lead PV Associate on moderate to...
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Associate II, Pharmacovigilance
Há 1 dia
Mogi das Cruzes, State of São Paulo, Brasil Worldwide Clinical Trials Tempo integralWhat 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 instructions. Serves as Lead PV Associate on moderate to...
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Associate II, Pharmacovigilance
Há 1 dia
Vespasiano, Minas Gerais, Brasil Worldwide Clinical Trials Tempo integralWhat 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 instructions. Serves as Lead PV Associate on moderate to...
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Associate II, Pharmacovigilance
Há 1 dia
Caruaru, Pernambuco, Brasil Worldwide Clinical Trials Tempo integralWhat 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 instructions. Serves as Lead PV Associate on moderate to...
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Associate II, Pharmacovigilance
Há 1 dia
Montenegro, Rio Grande do Sul, Brasil Worldwide Clinical Trials Tempo integralWhat 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 instructions. Serves as Lead PV Associate on moderate to...
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Associate II, Pharmacovigilance
Há 1 dia
Timon, State of Maranhão, Brasil Worldwide Clinical Trials Tempo integralWhat 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 instructions. Serves as Lead PV Associate on moderate to...
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Associate II, Pharmacovigilance
Há 1 dia
Alvorada, Rio Grande do Sul, Brasil Worldwide Clinical Trials Tempo integralWhat 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 instructions. Serves as Lead PV Associate on moderate to...
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Associate II, Pharmacovigilance
Há 1 dia
Fazenda Rio Grande, Paraná, Brasil Worldwide Clinical Trials Tempo integralWhat 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 instructions. Serves as Lead PV Associate on moderate to...
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Associate II, Pharmacovigilance
Há 1 dia
Ribeirão Pires, State of São Paulo, Brasil Worldwide Clinical Trials Tempo integralWhat 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 instructions. Serves as Lead PV Associate on moderate to...
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Associate II, Pharmacovigilance
Há 1 dia
Castanhal, Pará, Brasil Worldwide Clinical Trials Tempo integralWhat 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 instructions. Serves as Lead PV Associate on moderate to...
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Associate II, Pharmacovigilance
Há 1 dia
Maceió, Alagoas, Brasil Worldwide Clinical Trials Tempo integralWhat 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 instructions. Serves as Lead PV Associate on moderate to...
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Associate II, Pharmacovigilance
Há 1 dia
Rondonópolis, Mato Grosso, Brasil Worldwide Clinical Trials Tempo integralWhat 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 instructions. Serves as Lead PV Associate on moderate to...
