23/05/2024 | Fulltime | | United States | CV-Library | £14 / Hour Or require assistance or reasonable adjustments to be made for you during the selection process due to disability or long-term health condition, we will do our best to assist you. If you want to register your interest and apply, please contact me on the below Miren Chauhan Delivery Consultant Email (url
Save for laterRegister your CV22/05/2024 | Fulltime | Kaiserslautern | 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 | Kaiserslautern | 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 | Kaiserslautern | 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 | Kaiserslautern | 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 | Kaiserslautern | 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 | Kaiserslautern | 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 | Kaiserslautern | 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 | Kaiserslautern | 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 | Kaiserslautern | 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
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