21.05.24 | Vollzeit | Freising | 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 | München | 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 ansehen21.05.24 | Vollzeit | München | 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 ansehen21.05.24 | Vollzeit | Landshut | 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 | München | 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 | Erding | 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 | Friedberg | 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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