06/06/2024 | Fulltime | Cambridge | BioNTech SEHealth authority questions (FDA, EMA) and in leadings statistics on regulatory submissions, including developing ISE/ISS packages Good knowledge and experience of clinical development, study designs, advanced statistical methods (adaptive design and/or Bayesian is a plus), regulatory guidelines (ICH, FDA
Save for later06/06/2024 | 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 later06/06/2024 | 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 later06/06/2024 | Fulltime | Cambridge | BioNTech SEHealth authority questions (FDA, EMA) and in leadings statistics on regulatory submissions, including developing ISE/ISS packages Good knowledge and experience of clinical development, study designs, advanced statistical methods (adaptive design and/or Bayesian is a plus), regulatory guidelines (ICH, FDA
Save for later06/06/2024 | 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 later06/06/2024 | 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 later06/06/2024 | Fulltime | Cambridge | BioNTech SEHealth authority questions (FDA, EMA) and in leadings statistics on regulatory submissions, including developing ISE/ISS packages Good knowledge and experience of clinical development, study designs, advanced statistical methods (adaptive design and/or Bayesian is a plus), regulatory guidelines (ICH, FDA
Save for later06/06/2024 | 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 later06/06/2024 | Fulltime | Cambridge | BioNTech SEOngoing pipeline expansion Generate ad hoc data sets and TLFs on ongoing basis BSc or MSc in Statistics, Mathematics, Computer Science or related subjects 10+ years of experience in the pharmaceutical industry and/or CRO Excellent knowledge of statistical programming in SAS including Base, Macro, STAT
Save for later04/06/2024 | Fulltime | Cambridge | BioNTech SEDevelopment Bachelor´s degree in Statistics, Mathematics, Computer Science or related discipline, advanced degree preferred 10+ years (5+ years for advanced degree) experience in a pharmaceutical industry, CRO or another clinical research setting Excellent knowledge of statistical programming including SAS
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