22/05/2024 | 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 later23/05/2024 | Fulltime | Rochester | CV-Library | £38,000 - £44,000 / Year Boards (PCBs) The key duties for this role include Carrying out First Article Inspections on PCBs, bare and assembled. Responsibility for investigating customer quality concerns and writing reports on results. Communicating contractual quality requirements to the assembly team and ensuring adherence
Save for laterRegister your CV22/05/2024 | Fulltime | Swindon | CV-Library | £38,000 - £40,000 / Year Contract Manager for our client in Swindon. Responsible for managing the organisation's daily operational functions. That involves planning and implementing operational processes to improve quality, productivity, cost control and performance. The Contract Manager is to oversee all client
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