data entry

1,000 vagas de data entry em Brasil. Encontre vagas atualizadas diariamente.


  • Primavera do Leste, Mato Grosso, Brasil Worldwide Clinical Trials Tempo integral

    What 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...


  • Petrolina, Pernambuco, Brasil Worldwide Clinical Trials Tempo integral

    What 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...


  • Maracanaú, Ceará, Brasil Worldwide Clinical Trials Tempo integral

    What 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...


  • Rio de Janeiro, Rio de Janeiro, Brasil Samba TV Tempo integral R$ 392.927 - R$ 589.390 Contrato

    OverviewSamba is a media intelligence company. We know what the world is watching, reading, and thinking about in real time, at scale, across every screen. Our data exists with the consent of over a billion people, organized into the most complete picture of consumer attention ever built. The biggest brands in the world use that picture to make smarter...


  • Brasília, Federal District, Brasil OperationsArmy Remoto Tempo integral

    Job Title: Accounting AI AnalystSchedule: Full-Time, 45 hours/weekWork Days: Monday to FridayWork Hours: Staggered shifts between 8:00 AM to 8:00 PM ESTWork Setup: Fully Remote Apply here: https://operationsarmy.com/application About the Role Were looking for highly detail-oriented Accounting AI Analyst to support our AI operations team. In this role,...

  • Cybersecurity Analyst I Premium

    Há 5 horas


    BRA SAOP 215, Brasil FIS Capital Markets Tempo integral

    Monitor security alerts and escalate incidents as per defined protocols. Assist in vulnerability scans and patch verification. Document findings and maintain security logs. Support compliance checks and audit preparation. Learn and apply cybersecurity best practices and tools.Entry-level technical role involving defined tasks under regular supervision. The...


  • Teresina, Piauí, Brasil Worldwide Clinical Trials Tempo integral

    What 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...


  • Rio Verde, Goiás, Brasil Worldwide Clinical Trials Tempo integral

    What 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...


  • Camaçari, Bahia, Brasil Worldwide Clinical Trials Tempo integral

    What 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...


  • Guarapuava, Paraná, Brasil Worldwide Clinical Trials Tempo integral

    What 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...


  • Natal, Rio Grande do Norte, Brasil Worldwide Clinical Trials Tempo integral

    What 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...


  • Boituva, State of São Paulo, Brasil Worldwide Clinical Trials Tempo integral

    What 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...


  • Juiz de Fora, Minas Gerais, Brasil Worldwide Clinical Trials Tempo integral

    What 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...


  • Pouso Alegre, Minas Gerais, Brasil Worldwide Clinical Trials Tempo integral

    What 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...


  • Brejo, Bahia, Brasil Worldwide Clinical Trials Tempo integral

    What 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...


  • Olinda, Pernambuco, Brasil Worldwide Clinical Trials Tempo integral

    What 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...


  • Arapongas, Paraná, Brasil Worldwide Clinical Trials Tempo integral

    What 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...


  • Sorriso, Mato Grosso, Brasil Worldwide Clinical Trials Tempo integral

    What 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...


  • Aquiraz, Ceará, Brasil Worldwide Clinical Trials Tempo integral

    What 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...


  • Capão da Canoa, State of Rio Grande do Sul, Brasil Worldwide Clinical Trials Tempo integral

    What 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...