06.06.24 | Vollzeit | Mannheim | 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 | Mannheim | BioNTech SEFor all statistical aspects Serve as the biostatistics lead core team member for all assigned programs 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
Später ansehen06.06.24 | Vollzeit | Mannheim | 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 | Mannheim | BioNTech SEFor all statistical aspects Serve as the biostatistics lead core team member for all assigned programs 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
Später ansehen06.06.24 | Vollzeit | Aschaffenburg | BioNTech SEFor statistical data analysis and reporting Independently perform or oversee the production and/or validation of programming deliverables (e.g., analysis datasets, tables, listings) for study reports and integrated summaries Anticipate resource needs and works with management to ensure adequate long-term resource
Später ansehen06.06.24 | Vollzeit | Worms | 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 | Darmstadt | 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 | Darmstadt | 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 | Wiesbaden | BioNTech SEFor statistical data analysis and reporting Independently perform or oversee the production and/or validation of programming deliverables (e.g., analysis datasets, tables, listings) for study reports and integrated summaries Anticipate resource needs and works with management to ensure adequate long-term resource
Später ansehenVerpassen Sie nie wieder einen passenden Job!
Alle Jobs für Quality Reporting in Worms Landkreis kostenlos abonnieren.