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
aquiraz, estado do 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 2 dias
lavras, 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
cabo frio, 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
caieiras, 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
três lagoas, 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 2 dias
boituva, 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
campina grande do sul, 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
francisco beltrão, 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
várzea 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
flores da cunha, 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 2 dias
guarapuava, 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 pires, 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
resende, 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
itabira, 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
castanhal, 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
guarapari, 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
itapecerica da serra, 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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Administrative Assistant Premium
Há 1 dia
Valparaiso, Para, Brasil Valdes Architecture & Engineering Tempo integral US$ 17 - US$ 25 EfetivoResponsibilities Makes decisions within the scope of the position and authority, as well as independent decisions regarding planning, organizing, and scheduling work for self Can also make decisions that have an impact on the department Provides administrative support to management or a team Work will include general duties such as: budget...
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Sales Manager Premium
Há 1 dia
Sao Paulo, Sao Paulo, Brasil LSports Tempo integralLSports is a world-leading sports data provider, trusted by sportsbooks worldwide to deliver real-time data with unmatched accuracy and reliability. With technology that drives smarter trading and deeper engagement, we empower bookmakers to grow, innovate, and stay ahead of the game.If you’re passionate about sports and technology and want to make your...
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Accounts Executive
Há 5 dias
Região Norte, Região Norte, Brasil CVista HR Consulting Pte Ltd Tempo integral R$ 56.000 - R$ 89.000 ContratoResponsibilitiesManage Accounts Receivable (AR) or Accounts Payable (AP), including monthly and yearly closing processesPrepare monthly cash flow statementsPrepare journal entries and perform data entryPrepare account schedulesPrepare financial statements for statutory and tax reporting purposesLiaise with external auditors, tax agents, company secretary,...