Empregos de save on dev em Setubal

15 vagas de save on dev em Portugal. Encontre vagas atualizadas diariamente.


  • Almada, Setubal, Portugal Acorai Tempo integral

    pAcorai AB in Portugal seeks a hands-on clinical research professional to run multicentre investigations validating the SAVE Sensor System. You will coordinate between sites, data, and regulatory requirements to ensure protocol compliance and high-quality evidence. You will design eCRFs, manage data, monitor site activities, prepare datasets, oversee ethics...


  • Costa da Caparica, Setubal, Portugal Acorai Tempo integral

    Acorai AB in Portugal seeks a hands-on clinical research professional to run multicentre investigations validating the SAVE Sensor System. You will coordinate between sites, data, and regulatory requirements to ensure protocol compliance and high-quality evidence. You will design eCRFs, manage data, monitor site activities, prepare datasets, oversee ethics...


  • Sesimbra, Setubal, Portugal Acorai Tempo integral

    Acorai AB in Portugal seeks a hands-on clinical research professional to run multicentre investigations validating the SAVE Sensor System. You will coordinate between sites, data, and regulatory requirements to ensure protocol compliance and high-quality evidence. You will design eCRFs, manage data, monitor site activities, prepare datasets, oversee ethics...


  • Sobreda, Setubal, Portugal Acorai Tempo integral

    pAcorai AB in Portugal seeks a hands-on clinical research professional to run multicentre investigations validating the SAVE Sensor System. You will coordinate between sites, data, and regulatory requirements to ensure protocol compliance and high-quality evidence. You will design eCRFs, manage data, monitor site activities, prepare datasets, oversee ethics...


  • Caparica, Setubal, Portugal Acorai Tempo integral

    pAcorai AB in Portugal seeks a hands-on clinical research professional to run multicentre investigations validating the SAVE Sensor System. You will coordinate between sites, data, and regulatory requirements to ensure protocol compliance and high-quality evidence. You will design eCRFs, manage data, monitor site activities, prepare datasets, oversee ethics...