08.05.24 | Vollzeit | Unterschleißheim | Daiichi Sankyo Europe GmbHSections of the Clinical Overview modules of submission dossier, Post Authorization Safety Studies (PASS) and non-interventional studies (NIS), CCDS, SmPC, responses to HA safety queries) Manages regulatory responses to emerging safety issues and provides strategies to address these, and follow-though
Später ansehen08.05.24 | Vollzeit | Unterschleißheim | Daiichi Sankyo Europe GmbHSections of the Clinical Overview modules of submission dossier, Post Authorization Safety Studies (PASS) and non-interventional studies (NIS), CCDS, SmPC, responses to HA safety queries) Manages regulatory responses to emerging safety issues and provides strategies to address these, and follow-though
Später ansehen08.05.24 | Vollzeit | Unterschleißheim | Daiichi Sankyo Europe GmbHSections of the Clinical Overview modules of submission dossier, Post Authorization Safety Studies (PASS) and non-interventional studies (NIS), CCDS, SmPC, responses to HA safety queries) Manages regulatory responses to emerging safety issues and provides strategies to address these, and follow-though
Später ansehen08.05.24 | Vollzeit | Unterschleißheim | Daiichi Sankyo Europe GmbHSections of the Clinical Overview modules of submission dossier, Post Authorization Safety Studies (PASS) and non-interventional studies (NIS), CCDS, SmPC, responses to HA safety queries) Manages regulatory responses to emerging safety issues and provides strategies to address these, and follow-though
Später ansehen08.05.24 | Vollzeit | Unterschleißheim | Daiichi Sankyo Europe GmbHSections of the Clinical Overview modules of submission dossier, Post Authorization Safety Studies (PASS) and non-interventional studies (NIS), CCDS, SmPC, responses to HA safety queries) Manages regulatory responses to emerging safety issues and provides strategies to address these, and follow-though
Später ansehen08.05.24 | Vollzeit | Unterschleißheim | Daiichi Sankyo Europe GmbHSections of the Clinical Overview modules of submission dossier, Post Authorization Safety Studies (PASS) and non-interventional studies (NIS), CCDS, SmPC, responses to HA safety queries) Manages regulatory responses to emerging safety issues and provides strategies to address these, and follow-though
Später ansehen08.05.24 | Vollzeit | Unterschleißheim | Daiichi Sankyo Europe GmbHSections of the Clinical Overview modules of submission dossier, Post Authorization Safety Studies (PASS) and non-interventional studies (NIS), CCDS, SmPC, responses to HA safety queries) Manages regulatory responses to emerging safety issues and provides strategies to address these, and follow-though
Später ansehen08.05.24 | Vollzeit | Unterschleißheim | Daiichi Sankyo Europe GmbHSections of the Clinical Overview modules of submission dossier, Post Authorization Safety Studies (PASS) and non-interventional studies (NIS), CCDS, SmPC, responses to HA safety queries) Manages regulatory responses to emerging safety issues and provides strategies to address these, and follow-though
Später ansehen08.05.24 | Vollzeit | Unterschleißheim | Daiichi Sankyo Europe GmbHSections of the Clinical Overview modules of submission dossier, Post Authorization Safety Studies (PASS) and non-interventional studies (NIS), CCDS, SmPC, responses to HA safety queries) Manages regulatory responses to emerging safety issues and provides strategies to address these, and follow-though
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