06.06.24 | Vollzeit | Kaiserslautern | BioNTech SEAccountable for all statistical aspects Work as part of a collaborative, cross-functional team with members from other disciplines Provide statistical input into clinical development plans, clinical study protocols, clinical study reports, regulatory submission documents, and publications ensuring accurate
Später ansehen06.06.24 | Vollzeit | Mainz | BioNTech SEAccountable for all statistical aspects Work as part of a collaborative, cross-functional team with members from other disciplines Provide statistical input into clinical development plans, clinical study protocols, clinical study reports, regulatory submission documents, and publications ensuring accurate
Später ansehen06.06.24 | Vollzeit | Frankfurt am Main | BioNTech SEAccountable for all statistical aspects Work as part of a collaborative, cross-functional team with members from other disciplines Provide statistical input into clinical development plans, clinical study protocols, clinical study reports, regulatory submission documents, and publications ensuring accurate
Später ansehen06.06.24 | Vollzeit | Cambridge | BioNTech SEAccountable for all statistical aspects Work as part of a collaborative, cross-functional team with members from other disciplines Provide statistical input into clinical development plans, clinical study protocols, clinical study reports, regulatory submission documents, and publications ensuring accurate
Später ansehen06.06.24 | Vollzeit | Mainz | BioNTech SEAccountable for all statistical aspects Work as part of a collaborative, cross-functional team with members from other disciplines Provide statistical input into clinical development plans, clinical study protocols, clinical study reports, regulatory submission documents, and publications ensuring accurate
Später ansehen06.06.24 | Vollzeit | Ludwigshafen am Rhein | BioNTech SEAccountable for all statistical aspects Work as part of a collaborative, cross-functional team with members from other disciplines Provide statistical input into clinical development plans, clinical study protocols, clinical study reports, regulatory submission documents, and publications ensuring accurate
Später ansehen06.06.24 | Vollzeit | Mainz | BioNTech SEAccountable for all statistical aspects Work as part of a collaborative, cross-functional team with members from other disciplines Provide statistical input into clinical development plans, clinical study protocols, clinical study reports, regulatory submission documents, and publications ensuring accurate
Später ansehen06.06.24 | Vollzeit | Ludwigshafen am Rhein | BioNTech SEAccountable for all statistical aspects Work as part of a collaborative, cross-functional team with members from other disciplines Provide statistical input into clinical development plans, clinical study protocols, clinical study reports, regulatory submission documents, and publications ensuring accurate
Später ansehen06.06.24 | Vollzeit | Kaiserslautern | BioNTech SEAccountable for all statistical aspects Work as part of a collaborative, cross-functional team with members from other disciplines Provide statistical input into clinical development plans, clinical study protocols, clinical study reports, regulatory submission documents, and publications ensuring accurate
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