data entry operator
1,000 vagas de data entry operator em Brasil. Encontre vagas atualizadas diariamente.
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Associate II, Pharmacovigilance
Há 4 dias
Palhoça, 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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Senior Revenue Accountant – US GAAP
Há 6 dias
, Brasil inDrive Tempo integralAccounting Data Analyst — RevenueAs one of the top mobility companies in the world, we have been redefining the industry with innovative mobile technologies since 2013, driving us toward becoming a super app. Join us in our mission to combat global injustice.We are looking for an experienced accounting professional with strong technical and data skills to...
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Associate II, Pharmacovigilance
Há 1 dia
Fortaleza, State of Ceará, 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 1 dia
contagem, 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 1 dia
ribeirão preto, 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 1 dia
novo hamburgo, estado do rio grande do sul, 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 1 dia
vitória, 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 1 dia
campo grande, ms, estado de mato grosso do sul, 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 1 dia
londrina, 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 1 dia
são luís, estado do maranhão, 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 1 dia
são leopoldo, estado do rio grande do sul, 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 1 dia
juiz de fora, 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 1 dia
belém, pa, 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 1 dia
serra, 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 1 dia
piracicaba, 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 1 dia
cascavel pr, 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 1 dia
alvorada, estado do rio grande do sul, 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 1 dia
santos, 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 1 dia
mogi das cruzes, 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 1 dia
esteio, estado do rio grande do sul, 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...
