22/05/2024 | Fulltime | Wiesbaden | BioNTech SECross-functional team with members from other disciplines Provide statistical guidance into clinical development plans, clinical study protocols, clinical study reports, regulatory submission documents, and publications ensuring accurate deliverables Perform and/or verify sample size calculations Lead
Save for later22/05/2024 | Fulltime | Mainz | BioNTech SECross-functional team with members from other disciplines Provide statistical guidance into clinical development plans, clinical study protocols, clinical study reports, regulatory submission documents, and publications ensuring accurate deliverables Perform and/or verify sample size calculations Lead
Save for later22/05/2024 | Fulltime | Frankfurt am Main | BioNTech SECross-functional team with members from other disciplines Provide statistical guidance into clinical development plans, clinical study protocols, clinical study reports, regulatory submission documents, and publications ensuring accurate deliverables Perform and/or verify sample size calculations Lead
Save for later22/05/2024 | Fulltime | Worms | BioNTech SECross-functional team with members from other disciplines Provide statistical guidance into clinical development plans, clinical study protocols, clinical study reports, regulatory submission documents, and publications ensuring accurate deliverables Perform and/or verify sample size calculations Lead
Save for later22/05/2024 | Fulltime | Mainz | BioNTech SECross-functional team with members from other disciplines Provide statistical guidance into clinical development plans, clinical study protocols, clinical study reports, regulatory submission documents, and publications ensuring accurate deliverables Perform and/or verify sample size calculations Lead
Save for later22/05/2024 | Fulltime | Ludwigshafen am Rhein | BioNTech SECross-functional team with members from other disciplines Provide statistical guidance into clinical development plans, clinical study protocols, clinical study reports, regulatory submission documents, and publications ensuring accurate deliverables Perform and/or verify sample size calculations Lead
Save for later22/05/2024 | Fulltime | Frankfurt am Main | BioNTech SECross-functional team with members from other disciplines Provide statistical guidance into clinical development plans, clinical study protocols, clinical study reports, regulatory submission documents, and publications ensuring accurate deliverables Perform and/or verify sample size calculations Lead
Save for later22/05/2024 | Fulltime | Offenbach am Main | BioNTech SECross-functional team with members from other disciplines Provide statistical guidance into clinical development plans, clinical study protocols, clinical study reports, regulatory submission documents, and publications ensuring accurate deliverables Perform and/or verify sample size calculations Lead
Save for later22/05/2024 | Fulltime | Ludwigshafen am Rhein | BioNTech SECross-functional team with members from other disciplines Provide statistical guidance into clinical development plans, clinical study protocols, clinical study reports, regulatory submission documents, and publications ensuring accurate deliverables Perform and/or verify sample size calculations Lead
Save for later22/05/2024 | Fulltime | | Germany | CV-Library | £60,426 - £73,375 / Year Site inspections and audits to guarantee quality and safety. Collaborate with other engineering disciplines and project teams to deliver integrated solutions. Manage and coordinate with contractors and suppliers to ensure timely project delivery. Provide technical guidance and support throughout
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