04/06/2024 | Fulltime | Newark (MD) | BioNTech SEBase, Macro, STAT, GRAPH, SQL, etc. Solid understanding of FDA, EMA, ICH, and global regulations and guidelines Solid knowledge and experience of industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards Oncology or infectious disease therapeutic
Save for later04/06/2024 | Fulltime | Honolulu | BioNTech SEBase, Macro, STAT, GRAPH, SQL, etc. Solid understanding of FDA, EMA, ICH, and global regulations and guidelines Solid knowledge and experience of industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards Oncology or infectious disease therapeutic
Save for later04/06/2024 | Fulltime | Newark (IL) | BioNTech SEBase, Macro, STAT, GRAPH, SQL, etc. Solid understanding of FDA, EMA, ICH, and global regulations and guidelines Solid knowledge and experience of industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards Oncology or infectious disease therapeutic
Save for later04/06/2024 | Fulltime | München | BioNTech SEBase, Macro, STAT, GRAPH, SQL, etc. Solid understanding of FDA, EMA, ICH, and global regulations and guidelines Solid knowledge and experience of industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards Oncology or infectious disease therapeutic
Save for later04/06/2024 | Fulltime | Newark (CA) | BioNTech SEBase, Macro, STAT, GRAPH, SQL, etc. Solid understanding of FDA, EMA, ICH, and global regulations and guidelines Solid knowledge and experience of industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards Oncology or infectious disease therapeutic
Save for later04/06/2024 | Fulltime | Glasgow | BioNTech SEBase, Macro, STAT, GRAPH, SQL, etc. Solid understanding of FDA, EMA, ICH, and global regulations and guidelines Solid knowledge and experience of industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards Oncology or infectious disease therapeutic
Save for later04/06/2024 | Fulltime | Honolulu | BioNTech SEBase, Macro, STAT, GRAPH, SQL, etc. Solid understanding of FDA, EMA, ICH, and global regulations and guidelines Solid knowledge and experience of industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards Oncology or infectious disease therapeutic
Save for later04/06/2024 | Fulltime | Newark (IL) | BioNTech SEBase, Macro, STAT, GRAPH, SQL, etc. Solid understanding of FDA, EMA, ICH, and global regulations and guidelines Solid knowledge and experience of industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards Oncology or infectious disease therapeutic
Save for later04/06/2024 | Fulltime | Wolverhampton | BioNTech SEBase, Macro, STAT, GRAPH, SQL, etc. Solid understanding of FDA, EMA, ICH, and global regulations and guidelines Solid knowledge and experience of industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards Oncology or infectious disease therapeutic
Save for later30/05/2024 | Fulltime | Birmingham | CV-LibraryEncompasses education, residential care and the clinical team To monitor progress and targets to ensure that each individual student can achieve planned outcomes Essential criteria Relevant experience of teaching pupils and young people with Autistic spectrum condition and/or challenging behaviours Relevant
Save for laterRegister your CVDon't you miss a job ever again!
Subscribe to all Clinical Trial Manager jobs in West Midlands County.