24.04.24 | Teilzeit, Vollzeit | Hamburg | AbbVie Deutschland GmbH & Co. KGDisciplines to advance medicines to our patients. This means Statistical planning, design, analysis, and reporting related to clinical studies and other scientific research studies, including review and development of relevant study and project documents Interaction with regulatory agencies Co-ordination
Später ansehen24.04.24 | Teilzeit, Vollzeit | Hamburg | AbbVie Deutschland GmbH & Co. KGDisciplines to advance medicines to our patients. This means Statistical planning, design, analysis, and reporting related to clinical studies and other scientific research studies, including review and development of relevant study and project documents Interaction with regulatory agencies Co-ordination
Später ansehen26.02.24 | Vollzeit | Hamburg | JobLeads GmbH | 125.000 € - 150.000 € In Engineering, Medicine or Science - 5+ years work experience in the regulatory environment of ISO 13485, MDR, MDSAP or ISO/IEC 17021-1 - We hire for mindset! Forward-thinking mindset and an understanding of the Notified Body environment - Highly developed communication skills (German and English) - Highly
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