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 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 oncology or infectious diseases trials from phase I-IV, including scientific publications Experience in leading to health authority questions (FDA, EMA) and in leadings statistics on regulatory submissions, including developing ISE/ISS packages Very good knowledge and experience of clinical development
Save for later19/03/2024 | Fulltime | Cambridge | BioNTech SEFor advanced degree) experience in a pharmaceutical industry, CRO or another clinical research setting Strong competence in statistical programming including SAS/Base, Macro, STAT, GRAPH, SQL, etc. Good understanding of FDA, EMA, ICH, and global regulations and guidelines Solid knowledge and experience
Save for later19/03/2024 | Fulltime | Cambridge | BioNTech SEOf oncology or infectious diseases trials from phase I-IV, including scientific publications Experience in leading to health authority questions (FDA, EMA) and in leadings statistics on regulatory submissions, including developing ISE/ISS packages Very good knowledge and experience of clinical development
Save for later19/03/2024 | Fulltime | Cambridge | BioNTech SEOf oncology or infectious diseases trials from phase I-IV, including scientific publications Experience in leading to health authority questions (FDA, EMA) and in leadings statistics on regulatory submissions, including developing ISE/ISS packages Very good knowledge and experience of clinical development
Save for later19/03/2024 | Fulltime | Cambridge | BioNTech SEOf oncology or infectious diseases trials from phase I-IV, including scientific publications Experience in leading to health authority questions (FDA, EMA) and in leadings statistics on regulatory submissions, including developing ISE/ISS packages Very good knowledge and experience of clinical development
Save for later19/03/2024 | Fulltime | Cambridge | BioNTech SEOf oncology or infectious diseases trials from phase I-IV, including scientific publications Experience in leading to health authority questions (FDA, EMA) and in leadings statistics on regulatory submissions, including developing ISE/ISS packages Very good knowledge and experience of clinical development
Save for later19/03/2024 | Fulltime | Cambridge | BioNTech SEOf oncology or infectious diseases trials from phase I-IV, including scientific publications Experience in leading to health authority questions (FDA, EMA) and in leadings statistics on regulatory submissions, including developing ISE/ISS packages Very good knowledge and experience of clinical development
Save for later19/03/2024 | Fulltime | Cambridge | BioNTech SEOf oncology or infectious diseases trials from phase I-IV, including scientific publications Experience in leading to health authority questions (FDA, EMA) and in leadings statistics on regulatory submissions, including developing ISE/ISS packages Very good knowledge and experience of clinical development
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