21.05.24 | Vollzeit | Friedberg | Daiichi Sankyo Europe GmbHAnd serving as the primary point of contact. Review and analyze data from clinical trials, post-marketing and other relevant sources for the prompt identification of safety signals. Review and evaluate serious adverse event reports from clinical trials or post-marketing for completeness, accuracy
Später ansehen21.05.24 | Vollzeit | Friedberg | Daiichi Sankyo Europe GmbHAnd serving as the primary point of contact. Review and analyze data from clinical trials, post-marketing and other relevant sources for the prompt identification of safety signals. Review and evaluate serious adverse event reports from clinical trials or post-marketing for completeness, accuracy
Später ansehen21.05.24 | Vollzeit | Unterschleißheim | Daiichi Sankyo Europe GmbHAnd serving as the primary point of contact. Review and analyze data from clinical trials, post-marketing and other relevant sources for the prompt identification of safety signals. Review and evaluate serious adverse event reports from clinical trials or post-marketing for completeness, accuracy
Später ansehen21.05.24 | Vollzeit | Rosenheim | Daiichi Sankyo Europe GmbHAnd serving as the primary point of contact. Review and analyze data from clinical trials, post-marketing and other relevant sources for the prompt identification of safety signals. Review and evaluate serious adverse event reports from clinical trials or post-marketing for completeness, accuracy
Später ansehen21.05.24 | Vollzeit | Friedberg | Daiichi Sankyo Europe GmbHAnd serving as the primary point of contact. Review and analyze data from clinical trials, post-marketing and other relevant sources for the prompt identification of safety signals. Review and evaluate serious adverse event reports from clinical trials or post-marketing for completeness, accuracy
Später ansehen21.05.24 | Vollzeit | Erding | Daiichi Sankyo Europe GmbHAnd serving as the primary point of contact. Review and analyze data from clinical trials, post-marketing and other relevant sources for the prompt identification of safety signals. Review and evaluate serious adverse event reports from clinical trials or post-marketing for completeness, accuracy
Später ansehen21.05.24 | Vollzeit | Fürstenfeldbruck | Daiichi Sankyo Europe GmbHAnd serving as the primary point of contact. Review and analyze data from clinical trials, post-marketing and other relevant sources for the prompt identification of safety signals. Review and evaluate serious adverse event reports from clinical trials or post-marketing for completeness, accuracy
Später ansehen21.05.24 | Vollzeit | Landshut | Daiichi Sankyo Europe GmbHAnd serving as the primary point of contact. Review and analyze data from clinical trials, post-marketing and other relevant sources for the prompt identification of safety signals. Review and evaluate serious adverse event reports from clinical trials or post-marketing for completeness, accuracy
Später ansehen21.05.24 | Vollzeit | Fürstenfeldbruck | Daiichi Sankyo Europe GmbHAnd serving as the primary point of contact. Review and analyze data from clinical trials, post-marketing and other relevant sources for the prompt identification of safety signals. Review and evaluate serious adverse event reports from clinical trials or post-marketing for completeness, accuracy
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