21.05.24 | Vollzeit | Unterschleißheim | Daiichi Sankyo Europe GmbHReview and evaluate serious adverse event reports from clinical trials or post-marketing for completeness, accuracy, expectedness and relatedness. Lead internal and external (especially regulatory, but also expert advisory) interactions to ensure quality outcomes in the risk evaluation and management
Später ansehen21.05.24 | Vollzeit | Unterschleißheim | Daiichi Sankyo Europe GmbHReview and evaluate serious adverse event reports from clinical trials or post-marketing for completeness, accuracy, expectedness and relatedness. Lead internal and external (especially regulatory, but also expert advisory) interactions to ensure quality outcomes in the risk evaluation and management
Später ansehen21.05.24 | Vollzeit | Unterschleißheim | Daiichi Sankyo Europe GmbHReview and evaluate serious adverse event reports from clinical trials or post-marketing for completeness, accuracy, expectedness and relatedness. Lead internal and external (especially regulatory, but also expert advisory) interactions to ensure quality outcomes in the risk evaluation and management
Später ansehen21.05.24 | Vollzeit | Unterschleißheim | Daiichi Sankyo Europe GmbHReview and evaluate serious adverse event reports from clinical trials or post-marketing for completeness, accuracy, expectedness and relatedness. Lead internal and external (especially regulatory, but also expert advisory) interactions to ensure quality outcomes in the risk evaluation and management
Später ansehen21.05.24 | Vollzeit | Unterschleißheim | Daiichi Sankyo Europe GmbHReview and evaluate serious adverse event reports from clinical trials or post-marketing for completeness, accuracy, expectedness and relatedness. Lead internal and external (especially regulatory, but also expert advisory) interactions to ensure quality outcomes in the risk evaluation and management
Später ansehen21.05.24 | Vollzeit | Unterschleißheim | Daiichi Sankyo Europe GmbHReview and evaluate serious adverse event reports from clinical trials or post-marketing for completeness, accuracy, expectedness and relatedness. Lead internal and external (especially regulatory, but also expert advisory) interactions to ensure quality outcomes in the risk evaluation and management
Später ansehen21.05.24 | Vollzeit | Unterschleißheim | Daiichi Sankyo Europe GmbHReview and evaluate serious adverse event reports from clinical trials or post-marketing for completeness, accuracy, expectedness and relatedness. Lead internal and external (especially regulatory, but also expert advisory) interactions to ensure quality outcomes in the risk evaluation and management
Später ansehen06.05.24 | Vollzeit | Unterschleißheim | Daiichi Sankyo Europe GmbHLead) Organize and prepare DS-representatives participation in key events, speeches, including e.g. production site visits by policy makers, round tables, and industry conferences Build and manage trustful relationships with stakeholders and institutions Fosters an open and creative information
Später ansehen06.05.24 | Vollzeit | Unterschleißheim | Daiichi Sankyo Europe GmbHLead) Organize and prepare DS-representatives participation in key events, speeches, including e.g. production site visits by policy makers, round tables, and industry conferences Build and manage trustful relationships with stakeholders and institutions Fosters an open and creative information
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