06/06/2024 | Fulltime | Kaiserslautern | BioNTech SEGRAPH, 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 Expertise in the requirements and technology required to support electronic submissions Experience in leading
Save for later06/06/2024 | Fulltime | Mainz | BioNTech SEGRAPH, 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 Expertise in the requirements and technology required to support electronic submissions Experience in leading
Save for later06/06/2024 | Fulltime | Cambridge | BioNTech SEGRAPH, 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 Expertise in the requirements and technology required to support electronic submissions Experience in leading
Save for later06/06/2024 | Fulltime | Frankfurt am Main | BioNTech SEGRAPH, 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 Expertise in the requirements and technology required to support electronic submissions Experience in leading
Save for later06/06/2024 | Fulltime | Frankfurt am Main | BioNTech SEGRAPH, 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 Expertise in the requirements and technology required to support electronic submissions Experience in leading
Save for later06/06/2024 | Fulltime | Hanau | BioNTech SEGRAPH, 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 Expertise in the requirements and technology required to support electronic submissions Experience in leading
Save for later06/06/2024 | Fulltime | Ludwigshafen am Rhein | BioNTech SEGRAPH, 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 Expertise in the requirements and technology required to support electronic submissions Experience in leading
Save for later06/06/2024 | Fulltime | Mannheim | BioNTech SEGRAPH, 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 Expertise in the requirements and technology required to support electronic submissions Experience in leading
Save for later19/06/2024 | Fulltime | London | CV-Library | £400 Develop, document, and execute manual test plans and scripts. - Utilise DataBricks for testing data pipelines and ensure data accuracy. - Perform automated testing using Selenium. - Write and execute SQL queries to validate data integrity. - Generate data reports and visualisations using Power BI
Save for laterRegister your CV21/06/2024 | Fulltime | Sutton (London) | CV-LibraryBusiness Development Manager to increase brand awareness, enhance local presence, and support our branch managers. This is a new role designed to drive referrals, enquiries, and SQLs, involving stakeholders, charities, and home care providers. So….If you're empathetic, customer-focused, and ready
Save for laterRegister your CV