19/03/2024 | Fulltime | Cambridge | BioNTech SEIn the pharmaceutical industry and/or CRO Excellent knowledge of statistical programming in SAS including Base, Macro, STAT, GRAPH, SQL Solid understanding of FDA, EMA, ICH and global regulations and industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards
Save for later19/03/2024 | Fulltime | Cambridge | 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 | Cambridge | 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 | Cambridge | BioNTech SEIn the pharmaceutical industry and/or CRO Excellent knowledge of statistical programming in SAS including Base, Macro, STAT, GRAPH, SQL Solid understanding of FDA, EMA, ICH and global regulations and industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards
Save for later19/03/2024 | Fulltime | Cambridge | 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 | Cambridge | 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 | Cambridge | BioNTech SEIn the pharmaceutical industry and/or CRO Excellent knowledge of statistical programming in SAS including Base, Macro, STAT, GRAPH, SQL Solid understanding of FDA, EMA, ICH and global regulations and industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards
Save for later19/03/2024 | Fulltime | Cambridge | 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 | Cambridge | BioNTech SEIn the pharmaceutical industry and/or CRO Excellent knowledge of statistical programming in SAS including Base, Macro, STAT, GRAPH, SQL Solid understanding of FDA, EMA, ICH and global regulations and industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards
Save for later19/03/2024 | Fulltime | Cambridge | BioNTech SEUnited, innovative, passionate. Get in touch with us if you are looking to be a part of creating hope for a healthy future in many people's lives. Director* Biostatistics Represent Statistics in all assigned cross-functional clinical study teams and other projects and holds him/herself accountable
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