13/04/2024 | Fulltime | Cambridge | Reed- UNLIMITEDE.g. Python, Java, Ruby, ) - experience using SQL to work with relational databases, ideally PostgreSQL - experience of working with a live production system
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16/04/2024 | Fulltime | Cambridge | CV-Library | £50,000 - £70,000 / Year Proficiency in using REST APIs and Python. Comfort with command-line interfaces. Experience in developing software requiring hospital IT approval. 2+ years of industry experience. Ability to communicate complex ideas clearly and effectively. Proficiency in SQL (PostgreSQL preferred). Experience working
Save for laterRegister your CV19/03/2024 | 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 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 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 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
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