data entry operator
1,000 vagas de data entry operator em Brasil. Encontre vagas atualizadas diariamente.
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Associate II, Pharmacovigilance
Há 2 dias
araçatuba, estado de são paulo, Brasil Worldwide Clinical Trials Tempo integralWhat the Associate II, Pharmacovigilance does at WorldwideResponsible 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 2 dias
olinda, estado de pernambuco, Brasil Worldwide Clinical Trials Tempo integralWhat the Associate II, Pharmacovigilance does at WorldwideResponsible 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 2 dias
campos dos goytacazes, estado do rio de janeiro, Brasil Worldwide Clinical Trials Tempo integralWhat the Associate II, Pharmacovigilance does at WorldwideResponsible 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 2 dias
fazenda rio grande, estado do paraná, Brasil Worldwide Clinical Trials Tempo integralWhat the Associate II, Pharmacovigilance does at WorldwideResponsible 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 2 dias
poços de caldas, estado de minas gerais, Brasil Worldwide Clinical Trials Tempo integralWhat the Associate II, Pharmacovigilance does at WorldwideResponsible 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 2 dias
ananindeua, estado do pará, Brasil Worldwide Clinical Trials Tempo integralWhat the Associate II, Pharmacovigilance does at WorldwideResponsible 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 2 dias
cachoeiro de itapemirim, estado do espírito santo, Brasil Worldwide Clinical Trials Tempo integralWhat the Associate II, Pharmacovigilance does at WorldwideResponsible 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 2 dias
arapiraca, estado de alagoas, Brasil Worldwide Clinical Trials Tempo integralWhat the Associate II, Pharmacovigilance does at WorldwideResponsible 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 2 dias
bragança paulista, estado de são paulo, Brasil Worldwide Clinical Trials Tempo integralWhat the Associate II, Pharmacovigilance does at WorldwideResponsible 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 2 dias
biguaçu, estado de santa catarina, Brasil Worldwide Clinical Trials Tempo integralWhat the Associate II, Pharmacovigilance does at WorldwideResponsible 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 2 dias
vitória da conquista, estado da bahia, Brasil Worldwide Clinical Trials Tempo integralWhat the Associate II, Pharmacovigilance does at WorldwideResponsible 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 2 dias
pato branco, estado do paraná, Brasil Worldwide Clinical Trials Tempo integralWhat the Associate II, Pharmacovigilance does at WorldwideResponsible 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 2 dias
ribeirão das neves, estado de minas gerais, Brasil Worldwide Clinical Trials Tempo integralWhat the Associate II, Pharmacovigilance does at WorldwideResponsible 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 2 dias
marabá, estado do pará, Brasil Worldwide Clinical Trials Tempo integralWhat the Associate II, Pharmacovigilance does at WorldwideResponsible 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 2 dias
paranaguá, estado do paraná, Brasil Worldwide Clinical Trials Tempo integralWhat the Associate II, Pharmacovigilance does at WorldwideResponsible 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 2 dias
sorriso, estado de mato grosso, Brasil Worldwide Clinical Trials Tempo integralWhat the Associate II, Pharmacovigilance does at WorldwideResponsible 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 2 dias
parauapebas, estado do pará, Brasil Worldwide Clinical Trials Tempo integralWhat the Associate II, Pharmacovigilance does at WorldwideResponsible 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 2 dias
ipojuca, estado de pernambuco, Brasil Worldwide Clinical Trials Tempo integralWhat the Associate II, Pharmacovigilance does at WorldwideResponsible 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 2 dias
salto, estado de são paulo, Brasil Worldwide Clinical Trials Tempo integralWhat the Associate II, Pharmacovigilance does at WorldwideResponsible 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 2 dias
vespasiano, estado de minas gerais, Brasil Worldwide Clinical Trials Tempo integralWhat the Associate II, Pharmacovigilance does at WorldwideResponsible 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...
