28.05.24 | Vollzeit | Mammendorf | Christian Mars GmbHDie Zusammenarbeit mit einem hochmotivierten, sympathischen und sehr erfolgreichen Team - Echtes Team-Feeling plus regelmäßige Events - Flache Hierarchie mit hoher Eigenverantwortung. - Kostenlose Parkplätze vor Ort, Getränke selbstverständlich auch inklusive - Attraktives Gehalt mit Raum nach oben (Entwicklung
Später ansehen21.05.24 | Vollzeit | Rosenheim | 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 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
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