06/06/2024 | Fulltime | Cambridge | 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
Save for later06/06/2024 | Fulltime | Cambridge | BioNTech SERelated to vendor overseeing, innovation in technologies, automation, processes, and standards to maximize efficiency in statistical analysis and reporting Build efficient processes, innovative solutions, and standards to ensure timely and quality deliverables, including design and infrastructure
Save for later06/06/2024 | Fulltime | Cambridge | BioNTech SERelated to vendor overseeing, innovation in technologies, automation, processes, and standards to maximize efficiency in statistical analysis and reporting Build efficient processes, innovative solutions, and standards to ensure timely and quality deliverables, including design and infrastructure
Save for later06/06/2024 | Fulltime | Cambridge | BioNTech SEGRAPH, SQL Solid understanding of FDA, EMA, ICH and global regulations and industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards Expertise in the requirements and technology required to support electronic submissions Experience in leading
Save for later06/06/2024 | Fulltime | Cambridge | BioNTech SEGRAPH, SQL Solid understanding of FDA, EMA, ICH and global regulations and industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards Expertise in the requirements and technology required to support electronic submissions Experience in leading
Save for later06/06/2024 | Fulltime | 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
Save for later06/06/2024 | Fulltime | 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
Save for later06/06/2024 | Fulltime | Cambridge | 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
Save for later06/06/2024 | Fulltime | Cambridge | 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
Save for later06/06/2024 | Fulltime | 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
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