Vacatures 131 tot 140 van 164 (ontdubbeld 163)
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Kpmg - Arnhem
Wat ga jij doen als Audit Associate - Arnhem?In jouw functie als audit associate sta je klaar om financiële verantwoordingen kritisch onder de loep te nemen, waaronder jaarcijfers en rapportages. Jij bekijkt de financiële- Volledige vacature bekijken
Kpmg - Maastricht
Wat ga jij doen als Audit Associate - Maastricht?In jouw functie als audit associate sta je klaar om financiële verantwoordingen kritisch onder de loep te nemen, waaronder jaarcijfers en rapportages. Jij bekijkt de- Volledige vacature bekijken
Clinical Project Manager / Sr Clinical Project Manager
United BioSource
Master File (TMF/eTMF) is maintained and audit-ready on ongoing basisMonitor and ensure project team compliance with maintenance of Clinical Trial Management System (CTMS) Completion of departmental oversight trackers for projects2 dagen geleden - Volledige vacature bekijken
Vacatures, Stoevelaar - Amsterdam
arbeidsvoorwaarden, architect, area, arts, afgestudeerden, areamanager, artsen, banen, assessment, artsenbezoekers, assistant, fysiotherapeuten, artsenorganisaties, assistent, biomedisch, bewegingswetenschappers, associate , assistenten- Opslaan
Rik van Dinteren Ik wil een steentje bijdragen aan e...
Novartis
veel plezier op deze afdeling als clinical research associate , ofwel CRA. Rik van Dinteren Kun je wat meer vertellen over jouw rol als CRA? “Ik ben een brugfiguur tussen Novartis en de lokale onderzoeksteams in de60+ dagen geleden - Preview - Opslaan
Disease mechanisms and new therapies background info...
Radboudumc - Rha
including GMP facilities such as clean rooms Disease models (towards human research models, organoids) Clinical trial facilities including outcome measures and support Develop methods to investigate the- Opslaan
Julius Clinical - Utrecht
all other Julius Clinical’s employees. How do you become a Project Manager at Julius Clinical ? The classical route is to enter the industry as a Clinical Trial Assistant (CTA) or Clinical Research Associate (CRA- Preview - Opslaan
Regulatory Affairs Specialist - Dossier Development
Oxfordcorp - Leiden
responsible for all issues regarding CMC. Responsibilities Coordinate and provide technical oversight for the generation of the CMC dossier of marketing and clinical trial submission. Develop the technical eCTD sections- Opslaan
Study Start Up Associate I - Dutch Speaker
Icon Plc - Utrecht
mission to shape the future of clinical development. We are currently seeking a Study Start Up Associate I to join our diverse and dynamic team. As a Study Start Up Associate II at ICON, you will play a pivotal role in leading- Preview - Opslaan
Clinical Contracts & Budgets Associate
Oxfordcorp
Don't hesitate and apply today! Job Description As a Clinical Contracts & Budgets Associate , you will be providing clinical site contracting services to clinical study teams to support study start up and conduct activities60+ dagen geleden - Preview - Opslaan
Study Start Up Associate I - Dutch Speaker
Icon Plc - Utrecht
similar roles below... Study Start Up Associate I - Netherlands, Utrecht, Zen ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving- Preview - Opslaan
Scientist Immunology / Biomarkers
Oxfordcorp - Leiden
efficacy. In addition, manufacturing processes are optimized and established, and the resulting clinical trial material is evaluated in human clinical studies. The biomarker immuno team supports the vaccine development team in- Preview - Opslaan