21.03.24 | Vollzeit | Rüsselsheim | BioNTech SETo the integrated development plan, clinical development plan, and to regulatory study- or program-related documents such as clinical trial protocols, and -reports, investigator brochures, briefing documents, and market authorization applications Contributes to the execution of the translational and biomarker
Später ansehen21.03.24 | Vollzeit | Rüsselsheim | BioNTech SETo the integrated development plan, clinical development plan, and to regulatory study- or program-related documents such as clinical trial protocols, and -reports, investigator brochures, briefing documents, and market authorization applications Contributes to the execution of the translational and biomarker
Später ansehen21.03.24 | Vollzeit | Rüsselsheim | BioNTech SETo the integrated development plan, clinical development plan, and to regulatory study- or program-related documents such as clinical trial protocols, and -reports, investigator brochures, briefing documents, and market authorization applications Contributes to the execution of the translational and biomarker
Später ansehen21.03.24 | Vollzeit | Rüsselsheim | BioNTech SETo the integrated development plan, clinical development plan, and to regulatory study- or program-related documents such as clinical trial protocols, and -reports, investigator brochures, briefing documents, and market authorization applications Contributes to the execution of the translational and biomarker
Später ansehen21.03.24 | Vollzeit | Rüsselsheim | BioNTech SETo the integrated development plan, clinical development plan, and to regulatory study- or program-related documents such as clinical trial protocols, and -reports, investigator brochures, briefing documents, and market authorization applications Contributes to the execution of the translational and biomarker
Später ansehen21.03.24 | Vollzeit | Rüsselsheim | BioNTech SETo the integrated development plan, clinical development plan, and to regulatory study- or program-related documents such as clinical trial protocols, and -reports, investigator brochures, briefing documents, and market authorization applications Contributes to the execution of the translational and biomarker
Später ansehen21.03.24 | Vollzeit | Rüsselsheim | BioNTech SETo the integrated development plan, clinical development plan, and to regulatory study- or program-related documents such as clinical trial protocols, and -reports, investigator brochures, briefing documents, and market authorization applications Contributes to the execution of the translational and biomarker
Später ansehen21.03.24 | Vollzeit | Rüsselsheim | BioNTech SETo the integrated development plan, clinical development plan, and to regulatory study- or program-related documents such as clinical trial protocols, and -reports, investigator brochures, briefing documents, and market authorization applications Contributes to the execution of the translational and biomarker
Später ansehen21.03.24 | Vollzeit | Rüsselsheim | BioNTech SETo the integrated development plan, clinical development plan, and to regulatory study- or program-related documents such as clinical trial protocols, and -reports, investigator brochures, briefing documents, and market authorization applications Contributes to the execution of the translational and biomarker
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