Job offers for Clinical Trial Manager jobs in Hertfordshire County

07/06/2024 | Fulltime | Hatfield (Hertfordshire) | CV-LibraryCK Group are recruiting for a Manager, Global Clinical Trial Transparency and Disclosure with a well-established and successful global pharmaceutical Company based in Hatfield, Hertfordshire on a fixed term contract basis for 12 months. Manager Role To ensure compliance with the disclosure

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

04/06/2024 | 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

04/06/2024 | 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

04/06/2024 | 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

04/06/2024 | 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

04/06/2024 | 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

04/06/2024 | 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

04/06/2024 | 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

04/06/2024 | 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