05.06.24 | Vollzeit | München | Daiichi Sankyo Europe GmbHSafety team, and be responsible for overall product safety strategy or specific areas of safety surveillance and risk management, and provide safety leadership including but not limited to clinical studies, post-marketing surveillance, signal detection and management, important safety topics
Später ansehen21.05.24 | Vollzeit | Dachau | 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 | Dachau | 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 | Landsberg am Lech | 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 ansehenVerpassen Sie nie wieder einen passenden Job!
Alle Jobs für Event Management in München Landkreis kostenlos abonnieren.