data entry representative
1,000 vagas de data entry representative em Brasil. Encontre vagas atualizadas diariamente.
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Associate II, Pharmacovigilance
Há 1 dia
araras, 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
arujá, 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
garibaldi, 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
votorantim, 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
franco da rocha, 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
dois irmãos, 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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Sr Sales Operations Manager
Há 2 dias
Brasília, Região Centro-Oeste, Brasil Keeta Tempo integral R$ 180.000 - R$ 240.000 ContratoAbout the RoleWe are seeking an experienced Senior Sales Operations Manager (IC) to join our team as the strategic engine behind our SMB merchant growth. Although this position carries a Manager title, it is a hands‑on Individual Contributor (IC) role at the intersection of Sales Operations, Go‑To‑Market (GTM) Strategy, and Analytics.Key...
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Dynamics CE Senior Developer
Há 1 dia
Belo Horizonte, Minas Gerais, Brasil Nearsure Remoto Tempo integral R$ 371.550 - R$ 477.707 ContratoOverview Dynamics CE Senior Developer - Work from home We are a LATAM remote team that values autonomy, open communication, and respect for diversity. Our People Care team supports you from day one, and our Accounts Management team ensures smooth client relationships so you can focus on what you do best. What we offer Competitive USD salary 100% remote work...
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Associate II, Pharmacovigilance
Há 1 dia
distrito federal, distrito federal, 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
cuiabá, 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 1 dia
joão pessoa, estado da paraíba, 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
blumenau, 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 1 dia
itajaí, 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 1 dia
sorocaba, 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
são josé dos campos, 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
cachoeirinha, rs, 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
estado de mato grosso do sul, 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
anápolis, estado de goiás, 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 josé do rio 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
balneário camboriú, 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...
