19/03/2024 | Fulltime | Kaiserslautern | BioNTech SEAnd reporting on clinical trials, including CDISC standards Expertise in the requirements and technology required to support electronic submissions Experience in leading submissions and managing people Oncology or Infectious Disease therapeutic areas and submission experience is preferred Strong leadership
Save for later19/03/2024 | Fulltime | Kaiserslautern | BioNTech SEAnd reporting on clinical trials, including CDISC standards Expertise in the requirements and technology required to support electronic submissions Experience in leading submissions and managing people Oncology or Infectious Disease therapeutic areas and submission experience is preferred Strong leadership
Save for later19/03/2024 | Fulltime | Kaiserslautern | BioNTech SEAnd reporting on clinical trials, including CDISC standards Expertise in the requirements and technology required to support electronic submissions Experience in leading submissions and managing people Oncology or Infectious Disease therapeutic areas and submission experience is preferred Strong leadership
Save for later19/03/2024 | Fulltime | Kaiserslautern | BioNTech SEAnd reporting on clinical trials, including CDISC standards Expertise in the requirements and technology required to support electronic submissions Experience in leading submissions and managing people Oncology or Infectious Disease therapeutic areas and submission experience is preferred Strong leadership
Save for later19/03/2024 | Fulltime | Kaiserslautern | BioNTech SEAnd reporting on clinical trials, including CDISC standards Expertise in the requirements and technology required to support electronic submissions Experience in leading submissions and managing people Oncology or Infectious Disease therapeutic areas and submission experience is preferred Strong leadership
Save for later19/03/2024 | Fulltime | Kaiserslautern | BioNTech SEAnd reporting on clinical trials, including CDISC standards Expertise in the requirements and technology required to support electronic submissions Experience in leading submissions and managing people Oncology or Infectious Disease therapeutic areas and submission experience is preferred Strong leadership
Save for later19/03/2024 | Fulltime | Kaiserslautern | BioNTech SEAnd reporting on clinical trials, including CDISC standards Expertise in the requirements and technology required to support electronic submissions Experience in leading submissions and managing people Oncology or Infectious Disease therapeutic areas and submission experience is preferred Strong leadership
Save for later19/03/2024 | Fulltime | Kaiserslautern | BioNTech SEAnd reporting on clinical trials, including CDISC standards Expertise in the requirements and technology required to support electronic submissions Experience in leading submissions and managing people Oncology or Infectious Disease therapeutic areas and submission experience is preferred Strong leadership
Save for later19/03/2024 | Fulltime | Kaiserslautern | BioNTech SEAnd reporting on clinical trials, including CDISC standards Expertise in the requirements and technology required to support electronic submissions Experience in leading submissions and managing people Oncology or Infectious Disease therapeutic areas and submission experience is preferred Strong leadership
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17/04/2024 | Fulltime | Cambridge | CV-LibraryRequired ahead of regulatory approval, product launch, and mass manufacturing. You will be heavily involved in readying the company's product for clinical trial, and the verification and validation test plans and protocols for the product, documenting all activities within the Quality Management System
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