Job offers for Clinical Trial Manager jobs in England Country

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

24/05/2024 | Fulltime | Aberdeen | CV-Library | £45,000 / Year Clinical Trials Manager to join our Clinical and Application Research department. You will be responsible for all aspects of clinical trial management. The post holder will have a significant level of responsibility. Duties will include designing plus authoring trial documentation and regulatory

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 | Aschaffenburg | BioNTech SEAnd submission experience is preferred. Project management experience. Strong 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. BioNTech

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 | Offenbach am Main | BioNTech SEAnd submission experience is preferred. Project management experience. Strong 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. BioNTech

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