19/03/2024 | Fulltime | Kaiserslautern, Cambridge, Dar | 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 | Ludwigshafen am Rhein, Mainz | 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. Manager* Statistical Programming Work collaboratively with Clinical Development team or CRO to meet project deliverables and timelines for statistical data
Save for later19/03/2024 | Fulltime | Frankfurt am Main, Offenbach a | 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 | Aschaffenburg, Kaiserslautern | 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. Manager* Statistical Programming Work collaboratively with Clinical Development team or CRO to meet project deliverables and timelines for statistical data
Save for later19/03/2024 | Fulltime | Aschaffenburg, Kaiserslautern | 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. Manager* Statistical Programming Work collaboratively with Clinical Development team or CRO to meet project deliverables and timelines for statistical data
Save for later19/03/2024 | Fulltime | Frankfurt am Main, Offenbach a | 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. Manager* Statistical Programming Work collaboratively with Clinical Development team or CRO to meet project deliverables and timelines for statistical data
Save for later19/03/2024 | Fulltime | Cambridge, Darmstadt, Offenbac | 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 | Kaiserslautern, Aschaffenburg | 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. Manager* Statistical Programming Work collaboratively with Clinical Development team or CRO to meet project deliverables and timelines for statistical data
Save for later19/03/2024 | Fulltime | Frankfurt am Main, Offenbach a | 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 | Offenbach am Main, Frankfurt a | 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. Manager* Statistical Programming Work collaboratively with Clinical Development team or CRO to meet project deliverables and timelines for statistical data
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