data entry operator

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


  • lagoa santa, estado de minas gerais, Brasil Worldwide Clinical Trials Tempo integral

    What 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...


  • mogi mirim, estado de são paulo, Brasil Worldwide Clinical Trials Tempo integral

    What 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...


  • araras, estado de são paulo, Brasil Worldwide Clinical Trials Tempo integral

    What 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...


  • garibaldi, estado do rio grande do sul, Brasil Worldwide Clinical Trials Tempo integral

    What 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...


  • votorantim, estado de são paulo, Brasil Worldwide Clinical Trials Tempo integral

    What 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...


  • franco da rocha, estado de são paulo, Brasil Worldwide Clinical Trials Tempo integral

    What 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...


  • dois irmãos, estado do rio grande do sul, Brasil Worldwide Clinical Trials Tempo integral

    What 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...


  • lauro de freitas, estado da bahia, Brasil Worldwide Clinical Trials Tempo integral

    What 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...


  • agudos, estado de são paulo, Brasil Worldwide Clinical Trials Tempo integral

    What 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...


  • guarulhos, estado de são paulo, Brasil Worldwide Clinical Trials Tempo integral

    What 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...


  • feira de santana, estado da bahia, Brasil Worldwide Clinical Trials Tempo integral

    What 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...


  • hortolândia, estado de são paulo, Brasil Worldwide Clinical Trials Tempo integral

    What 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...


  • jandira, estado de são paulo, Brasil Worldwide Clinical Trials Tempo integral

    What 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...


  • arujá, estado de são paulo, Brasil Worldwide Clinical Trials Tempo integral

    What 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...


  • timon, estado do maranhão, Brasil Worldwide Clinical Trials Tempo integral

    What 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...

  • Product Expert

    Há 2 dias


    Curitiba, Paraná, Brasil Concentrix Tempo integral R$ 33.480 - R$ 55.800 Contrato

    Join to apply for the Product Expert role at Concentrix Responsibilities Prepare quotes, contracts, and RFP/RFI responses Maintain quote documentation with accurate pricing and configurations Maintain sales demonstration tools and applications in support of sales teams Work within a few sources of data/systems to produce an outcome with some...


  • , Brasil Crossing Hurdles Remoto Tempo integral R$ 6.800 - R$ 9.700 Contrato

    Position: Video Data Entry Specialist (LATAM)Type: Hourly contractCompensation: $6/hourLocation: RemoteCommitment: 10 40 hours/weekRole ResponsibilitiesCapture videos using a compatible smartphone while performing specified physical activities.Record video footage to ensure accurate and high-quality data collection.Follow project protocols and labeling...

  • Arrumadeira

    Há 5 dias


    Aparecida de Goiânia, Goiás, Brasil Vitlog Transportes Tempo integral R$ 20.000 - R$ 31.000 Contrato

    Arrumadeira Vitlog Transportes Processo seletivo presencial para arrumador de carga. Obs: as entrevistas vão acontecer no segundo prédio. Data e Horário Data: 07/07 Hora: 09h às 11h ou das 14h às 17h Leve o seu currículo e seja entrevistado na hora! Benefícios Seguro de vida Plano de saúde/odonto Gympass - Apoio pass Checkup saúde Desc. Farma Vale...


  • distrito federal, distrito federal, Brasil Worldwide Clinical Trials Tempo integral

    What 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...


  • cuiabá, estado de mato grosso, Brasil Worldwide Clinical Trials Tempo integral

    What 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...