19/03/2024 | Fulltime | Kaiserslautern | BioNTech SEOf industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards Oncology or Infectious Disease therapeutic areas and submission experience is preferred Project management experience, detail-oriented, and strong organizational and communication skills
Save for later19/03/2024 | Fulltime | Kaiserslautern | BioNTech SEOf industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards Oncology or Infectious Disease therapeutic areas and submission experience is preferred Project management experience, detail-oriented, and strong organizational and communication skills
Save for later19/03/2024 | Fulltime | Kaiserslautern | BioNTech SEOf industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards Oncology or Infectious Disease therapeutic areas and submission experience is preferred Project management experience, detail-oriented, and strong organizational and communication skills
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 SEOf industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards Oncology or Infectious Disease therapeutic areas and submission experience is preferred Project management experience, detail-oriented, and strong organizational and communication skills
Save for later19/03/2024 | Fulltime | Kaiserslautern | BioNTech SEOf industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards Oncology or Infectious Disease therapeutic areas and submission experience is preferred Project management experience, detail-oriented, and strong organizational and communication skills
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 SEOf industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards Oncology or Infectious Disease therapeutic areas and submission experience is preferred Project management experience, detail-oriented, and strong organizational and communication skills
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 SEOf industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards Oncology or Infectious Disease therapeutic areas and submission experience is preferred Project management experience, detail-oriented, and strong organizational and communication skills
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