computer

1,000 vagas de computer em Brasil. Encontre vagas atualizadas diariamente.


  • Mossoró, 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...


  • State of 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...


  • Timbó, Santa Catarina, 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...


  • Ribeirao Preto, 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...


  • Blumenau, State of Santa Catarina, 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...


  • Patos de Minas, 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...


  • 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...


  • Santa Luzia, 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...


  • São João do Jaboti, 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...


  • State of Santa Catarina, State of Santa Catarina, 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...


  • Ponta Grossa, 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...


  • Jacareí, 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...


  • Parauapebas, Pará, 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...


  • Varginha, 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...


  • Marabá, Pará, 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...


  • Bahia, Bahia, Brasil LatinHire Tempo integral R$ 111.044 - R$ 166.567 Contrato

    Cargo: College-level chemistry tutor em luis eduardo magalhães (BA) – luis eduardo magalhães Requisitos: We are looking for tutors to solve college-level Chemistry questions in English. These questions are submitted by students, who expect a response in less than 24 hours. In this project, tutors work in freelance mode and can decide the number of hours...


  • , Brasil LatinHire Tempo integral R$ 205.611 - R$ 342.686 Contrato

    Cargo College-level chemistry tutor em lages (CE) – lages Requisitos We are looking for tutors to solve college-level Chemistry questions in English. These questions are submitted by students, who expect a response in less than 24 hours. Tutors in this project work in freelance mode and can decide the number of hours they wish to work. Do you prefer to...


  • , Brasil LatinHire Tempo integral R$ 41.328 - R$ 82.656 Contrato

    Cargo:College-level chemistry tutor em eusébio (CE) – eusébioRequisitosWe are looking for tutors to solve college-level Chemistry questions in English. These questions are submitted by students, who expect a response in less than 24 hours. Tutors in this project work in freelance mode and can decide the number of hours they wish to work. Do you prefer to...


  • Lavras, State of 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...

  • Trainer

    Há 2 dias


    Propriá, Sergipe, Brasil Hitachi Rail Tempo integral

    As THE leader in transit technology, Hitachi Mobility Multimodal Solutions – Hitachi R ail vision is to make meaningful contributions to worldwide mobility. Our goal is to be the leading provider of exciting technology that improves the quality of mobility in communities around the world. We are continuing to grow, and are looking for a Trainer join...