data entry

4,443 vagas de data entry em Brasil. Encontre vagas atualizadas diariamente.


  • Marília, 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...


  • Santa Cruz do Sul, 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...


  • State of Espírito Santo, State of Espírito Santo, 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...


  • Mauá, 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...


  • State of Bahia, State of 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...


  • Flores da Cunha, 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...


  • Rio das Ostras, Rio de Janeiro, 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...


  • Cascavel, 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...


  • Araucária, 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...

  • Analista de pricing jr

    Há 21 horas


    Itajaí, Santa Catarina, Brasil Netvagas Tempo integral

    The junior analyst is responsible for qualifying shipment requests, coordinating with internal stakeholders, and ensuring accurate data entry and document issuance. They support the Sales teams by managing quotations, maintaining rate structures, and handling daily workflow operations. Effective communication, proactive problem-solving, and independent...


  • Rio de Janeiro, State of Rio de Janeiro, 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...


  • Salvador, State of 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...


  • São Paulo, São Paulo, Brasil Samba TV Tempo integral R$ 350.000 - R$ 520.000 Contrato

    Samba TV tracks streaming and broadcast video across the world with our proprietary data and technology. We are on a mission to fundamentally transform the viewing experience for everyone. Our data enables media companies to connect with audiences for new shows and movies, and enables advertisers to engage viewers and measure reach across all their devices....

  • Software Engineer

    Há 12 horas


    , Brasil Arete Studios Tempo integral R$ 120.000 - R$ 180.000 Contrato

    Company Description Arete Studios is an omnichannel discovery platform built for the next generation of fashion brands and Gen Z shoppers. The company enables cross-border growth for emerging designers by providing advanced data analytics tools that support market entry, production planning, and pricing decisions. A proprietary personalization engine...


  • 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...

  • Executive Assistant

    Há 2 dias


    Buenos Aires, Espírito Santo, Brasil Wing Assistant Remoto Tempo integral R$ 63.989 - R$ 96.277 Contrato

    Executive Assistant (Remote) Wing is on the exciting mission of redefining the future of work for companies worldwide! We are looking to be the one-stop shop for companies that are looking to build world-class teams & place their operations on autopilot. And we’re looking for an Executive Assistant to start immediately! Duties and Responsibilities Create...


  • São Bernardo do Campo, São Paulo, Brasil Jobtailor Tempo integral R$ 290.160 - R$ 424.080 Contrato

    ResponsibilitiesEnter and update control data in spreadsheets and internal systems.Perform administrative routines such as filing documents, managing forms, and maintaining cash records.Provide support in addressing inquiries from toll plazas regarding collection procedures.Assist with reconciliation of collected amounts (perform traffic validations).Support...


  • Viamão, 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...


  • Vila Velha, Espírito Santo, 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...


  • Viana, Espírito Santo, 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...