21.05.24 | Vollzeit | Rosenheim | Daiichi Sankyo Europe GmbHThe product life cycle. Effectively coordinate and manage available resources in developing and delivering high-quality safety evaluation related documents/deliverables on time. Coordinate and participate actively in safety-related regulatory interactions (e.g., regulatory meetings, post-approval commitments
Später ansehen21.05.24 | Vollzeit | Friedberg | Daiichi Sankyo Europe GmbHThe product life cycle. Effectively coordinate and manage available resources in developing and delivering high-quality safety evaluation related documents/deliverables on time. Coordinate and participate actively in safety-related regulatory interactions (e.g., regulatory meetings, post-approval commitments
Später ansehen21.05.24 | Vollzeit | Friedberg | Daiichi Sankyo Europe GmbHThe product life cycle. Effectively coordinate and manage available resources in developing and delivering high-quality safety evaluation related documents/deliverables on time. Coordinate and participate actively in safety-related regulatory interactions (e.g., regulatory meetings, post-approval commitments
Später ansehen21.05.24 | Vollzeit | Dachau | Daiichi Sankyo Europe GmbHThe product life cycle. Effectively coordinate and manage available resources in developing and delivering high-quality safety evaluation related documents/deliverables on time. Coordinate and participate actively in safety-related regulatory interactions (e.g., regulatory meetings, post-approval commitments
Später ansehen21.05.24 | Vollzeit | Dachau | Daiichi Sankyo Europe GmbHThe product life cycle. Effectively coordinate and manage available resources in developing and delivering high-quality safety evaluation related documents/deliverables on time. Coordinate and participate actively in safety-related regulatory interactions (e.g., regulatory meetings, post-approval commitments
Später ansehen21.05.24 | Vollzeit | Fürstenfeldbruck | Daiichi Sankyo Europe GmbHThe product life cycle. Effectively coordinate and manage available resources in developing and delivering high-quality safety evaluation related documents/deliverables on time. Coordinate and participate actively in safety-related regulatory interactions (e.g., regulatory meetings, post-approval commitments
Später ansehen08.05.24 | Vollzeit | Friedberg | Daiichi Sankyo Europe GmbHPhysician Specialty Medicines (m/f/x) The position Provides expertise in medical safety activities for the assigned projects - products including development of safety monitoring plan, effective implementation of safety monitoring activities, Benefit/Risk assessment with appropriate risk minimization
Später ansehen08.05.24 | Vollzeit | Germering | Daiichi Sankyo Europe GmbHPhysician Specialty Medicines (m/f/x) The position Provides expertise in medical safety activities for the assigned projects - products including development of safety monitoring plan, effective implementation of safety monitoring activities, Benefit/Risk assessment with appropriate risk minimization
Später ansehen08.05.24 | Vollzeit | Landshut | Daiichi Sankyo Europe GmbHPhysician Specialty Medicines (m/f/x) The position Provides expertise in medical safety activities for the assigned projects - products including development of safety monitoring plan, effective implementation of safety monitoring activities, Benefit/Risk assessment with appropriate risk minimization
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