06/06/2024 | Fulltime | Wiesbaden | 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 | Aschaffenburg | 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 | Mannheim | BioNTech SETo database requirements and work closely with Clinical Data Manager to ensure data quality standards are met PhD or Masters in (Bio)Statistics, Mathematics or equivalent Minimum 5 years (8 years for masters) in the pharmaceutical industry and/or CRO At least 3 years of work/leadership experience, overseeing
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 | Mainz | 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 | Mannheim | 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 | Darmstadt | BioNTech SETo database requirements and work closely with Clinical Data Manager to ensure data quality standards are met PhD or Masters in (Bio)Statistics, Mathematics or equivalent Minimum 5 years (8 years for masters) in the pharmaceutical industry and/or CRO At least 3 years of work/leadership experience, overseeing
Save for later06/06/2024 | Fulltime | Gaithersburg | 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 | Kaiserslautern | 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 later06/06/2024 | Fulltime | Kaiserslautern | 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
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