08.05.24 | Vollzeit | Friedberg | Daiichi Sankyo Europe GmbHMeetings and engages with colleagues in Medical affairs, Regulatory Affairs, Quality, etc, including participating in regulatory interactions Provide strategic guidance in the preparation of safety relevant parts of submission documents (e.g., CSR, Summary of Safety, B/R sections of the Clinical Overview
Später ansehen08.05.24 | Vollzeit | Friedberg | Daiichi Sankyo Europe GmbHMeetings and engages with colleagues in Medical affairs, Regulatory Affairs, Quality, etc, including participating in regulatory interactions Provide strategic guidance in the preparation of safety relevant parts of submission documents (e.g., CSR, Summary of Safety, B/R sections of the Clinical Overview
Später ansehen08.05.24 | Vollzeit | Friedberg | Daiichi Sankyo Europe GmbHMeetings and engages with colleagues in Medical affairs, Regulatory Affairs, Quality, etc, including participating in regulatory interactions Provide strategic guidance in the preparation of safety relevant parts of submission documents (e.g., CSR, Summary of Safety, B/R sections of the Clinical Overview
Später ansehen08.05.24 | Vollzeit | Friedberg | Daiichi Sankyo Europe GmbHMeetings and engages with colleagues in Medical affairs, Regulatory Affairs, Quality, etc, including participating in regulatory interactions Provide strategic guidance in the preparation of safety relevant parts of submission documents (e.g., CSR, Summary of Safety, B/R sections of the Clinical Overview
Später ansehen08.05.24 | Vollzeit | Friedberg | Daiichi Sankyo Europe GmbHMeetings and engages with colleagues in Medical affairs, Regulatory Affairs, Quality, etc, including participating in regulatory interactions Provide strategic guidance in the preparation of safety relevant parts of submission documents (e.g., CSR, Summary of Safety, B/R sections of the Clinical Overview
Später ansehen08.05.24 | Vollzeit | Friedberg | Daiichi Sankyo Europe GmbHMeetings and engages with colleagues in Medical affairs, Regulatory Affairs, Quality, etc, including participating in regulatory interactions Provide strategic guidance in the preparation of safety relevant parts of submission documents (e.g., CSR, Summary of Safety, B/R sections of the Clinical Overview
Später ansehen08.05.24 | Vollzeit | Friedberg | Daiichi Sankyo Europe GmbHMeetings and engages with colleagues in Medical affairs, Regulatory Affairs, Quality, etc, including participating in regulatory interactions Provide strategic guidance in the preparation of safety relevant parts of submission documents (e.g., CSR, Summary of Safety, B/R sections of the Clinical Overview
Später ansehen08.05.24 | Vollzeit | Friedberg | Daiichi Sankyo Europe GmbHMeetings and engages with colleagues in Medical affairs, Regulatory Affairs, Quality, etc, including participating in regulatory interactions Provide strategic guidance in the preparation of safety relevant parts of submission documents (e.g., CSR, Summary of Safety, B/R sections of the Clinical Overview
Später ansehen08.05.24 | Vollzeit | Friedberg | Daiichi Sankyo Europe GmbHMeetings and engages with colleagues in Medical affairs, Regulatory Affairs, Quality, etc, including participating in regulatory interactions Provide strategic guidance in the preparation of safety relevant parts of submission documents (e.g., CSR, Summary of Safety, B/R sections of the Clinical Overview
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