data entry

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


  • São Paulo, São Paulo, Brasil Jobtailor Tempo integral R$ 120.000 - R$ 180.000 Contrato

    Responsibilities Conduct high‑complexity internal audits in accordance with the Annual Audit Plan, within the established schedule. Prepare and document the planning for each audit based on the department's methodology and perform fieldwork. Contribute to work planning and execute audits to provide an independent, constructive assessment of Telefónica...

  • Clinical Data Manager Premium

    Há 2 semanas


    Rio de Janeiro, Rio de Janeiro, Brasil Precision Medicine Group Remoto Tempo integral

    We’re expanding across Mexico, Brazil, Argentina, Colombia, Chile, and Peru, and we’re looking for an experienced Clinical Data Manager to help build the foundation of our growing LATAM Data Management team, ensuring the delivery of high-quality clinical data that drives successful clinical trials and accelerates innovative therapies to patients....


  • são paulo, 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...


  • campinas, 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...


  • recife, estado de pernambuco, 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...


  • barueri, 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...


  • osasco, 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...


  • franca, 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...


  • paulínia, 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...


  • praia grande, 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...


  • toledo, estado do paraná, 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...


  • sumaré, sp, 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...


  • carapicuíba, 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...


  • luís eduardo magalhães, 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...


  • barretos, 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...


  • cabreúva, 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...


  • São Paulo, São Paulo, Brasil Mastercard Tempo integral R$ 120.000 - R$ 180.000 Contrato

    Mastercard’s People & Capability (P&C) Product organization is evolving toward an integrated, value driven product ecosystem that delivers a scalable, end to end employee experience across the hire to retire journey. We are seeking a highly analytical Compensation professional to oversee the mass processing and integration of compensation data into our...


  • Belo Horizonte, Minas Gerais, Brasil Nearsure Remoto Tempo integral R$ 371.550 - R$ 477.707 Contrato

    Overview 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...


  • 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...


  • ribeirão preto, 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...