10.05.24 | Vollzeit | Frankfurt am Main | KION GROUP AGOf data migration tests/trial loads to agreed levels of data volume and quality - With your expertise, you continuously improve and develop enterprise data quality and recognize changing business and industry requirements at an early stage and adapt data structures accordingly - You ensure Data Quality
Später ansehen14.05.24 | Vollzeit | Gräfelfing | FUTRUE GmbHMit unseren Fachabteilungen im Bereich Quality Assurance, Sales BI, Operations/Supply Chain, Clinical Trials, Grafik und Web Development zusammen. - Du steuerst und koordiniert die Zusammenarbeit mit unseren externen Dienstleistern im Bereich Marketing wie beispielsweise Media-Agenturen oder Druckereien
Später ansehen14.05.24 | Vollzeit | Eßlingen | BioTeSys GmbHDes Trial Master/Site File - Erstellung wissenschaftlicher englischsprachiger Studienunterlagen und Publikationen - Fähigkeit zum eigenverantwortlichen Arbeiten, zum konzeptionellen Denken und Übernahme von Projektverantwortung - Sie verfügen über ein abgeschlossenes naturwissenschaftliches Studium
Später ansehen01.04.24 | Vollzeit | München | JobLeads GmbH | 100.000 € - 125.000 € And post-study activities. Measures study progress against agreed upon timelines to milestones. • Ensure accurate budget management for assigned trials. This includes ensuring vendors and affiliate budgets are tracking according to plan. Updates are made to account for scope changes. • Ensure compliance
Später ansehen30.03.24 | Vollzeit | München | JobLeads GmbH | 100.000 € - 125.000 € Clinical Trials Management Associate Duration 06 Months Location Foster city, CA CTMA -Late Phase plays vital role in successful implementation and support of important Collaborative (CO) and Investigator-Sponsored Research (ISR) projects. Responsibilities Non-Client sponsored studies - Serves
Später ansehen29.03.24 | Vollzeit | München | JobLeads GmbH | 100.000 € - 125.000 € Operations - project team (i.e. Clinical Project Managers, Associate Directors, or Directors), in order - to facilitate the management of pre- and post-approval clinical trial processes including - quality review and document prep. - The CTA performs work within established protocols under general
Später ansehen14.05.24 | Vollzeit | Heidesheim am Rhein, Obrigheim | PAUL HARTMANN AGProspective clinical trials, real-world data, and evidence synthesis. As part of our dynamic team, you will play a key role in contributing to protocol development, evidence synthesis, clinical risk prediction (including machinge learning modeling) and various kind of quantitative research. This role offers
Später ansehen14.05.24 | Vollzeit | Ludwigshafen am Rhein | PAUL HARTMANN AGProspective clinical trials, real-world data, and evidence synthesis. As part of our dynamic team, you will play a key role in contributing to protocol development, evidence synthesis, clinical risk prediction (including machinge learning modeling) and various kind of quantitative research. This role offers
Später ansehen14.05.24 | Vollzeit | Mainz | PAUL HARTMANN AGProspective clinical trials, real-world data, and evidence synthesis. As part of our dynamic team, you will play a key role in contributing to protocol development, evidence synthesis, clinical risk prediction (including machinge learning modeling) and various kind of quantitative research. This role offers
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