12.05.24 | Vollzeit | Tübingen, Wiesbaden, Amsterdam | CureVac Corporate Services GmbHData storage systems focusing on MS Azure services (e.g., Data Factory, Synapse, Databricks) - Ensure data consistency and integrity during the integration process, performing data quality checks, data validation, and cleaning as needed - Monitor and tune data systems, identify and resolve performance
Später ansehen11.05.24 | Vollzeit | Putzbrunn | W. L. Gore & Associates GmbHImprovement and regulatory responses - Develop metrics for operational targets to monitor and evaluate regulatory compliance - Closely monitor and communicate performance to metrics, including insight into trends, alerts, and actions - Provide regulatory input for product recalls, recall communications
Später ansehen04.05.24 | Vollzeit | Monheim am Rhein | Elanco Animal Health GmbHAs the Director of Clinical Operations Europe, you will play a pivotal role in overseeing study support services and leading a dynamic team of 5 individuals. You will be responsible for driving excellence across three key areas monitoring and clinical research associate support, R&D study material logistics
Später ansehen16.05.24 | Vollzeit | Neu-Isenburg | GBG Forschungs GmbHMedical Advisor (m/w/d) Deine wesentlichen Aufgaben Betreuung von klinischen Studien mit Verantwortlichkeit für die medizinischen Inhalte und die Sicherheit der Patienten inkl. Medical Monitoring, Pharmakovigilanz und Bewertung von Referenzendokumenten Medizinische Beratung von externen
Später ansehen16.05.24 | Vollzeit | Neu-Isenburg | GBG Forschungs GmbHMedical Advisor (m/f/d) Your essential tasks Supervising clinical studies with responsibility for the medical content and patient safety, including medical monitoring, pharmacovigilance and evaluation of reference documents Giving medical advice to external study physicians and internal project
Später ansehen07.05.24 | Vollzeit | Hamburg | FUSE-AI GmbHAnd clinical indication - Competent in agile project development methodologies and project management (e.g. Jira, MS Project, etc.) - Competent in monitoring, maintenance and change control of software development in a regulated field - Competent in versioning, data logging and their visualization - Know-how
Später ansehen07.05.24 | Teilzeit | München | Philips GmbHZusammen mit den Projektmanager*innen an der klinischen Forschung im Bereich Advanced Hemodynamic Monitoring zu arbeiten. Du bist Teil des Clinical Affairs Teams und somit an der Durchführung klinischer Studien gemäß MDR, ISO 14155 und geltenden nationalen Rechtsvorschriften beteiligt
Später ansehen16.05.24 | Vollzeit | Kaiserslautern, Darmstadt, Lud | BioNTech SERequirements for trial-specific intended purposes of tests in our clinical programs. Monitoring of development activities and development plans of external diagnostic partners and alignment with BNT's clinical timelines Review partnership contracts to identify critical development and regulatory submission
Später ansehen16.05.24 | Vollzeit | Kaiserslautern, Darmstadt, Lud | BioNTech SERequirements for trial-specific intended purposes of tests in our clinical programs. Monitoring of development activities and development plans of external diagnostic partners and alignment with BNT's clinical timelines Review partnership contracts to identify critical development and regulatory submission
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