07/06/2024 | Fulltime | Hatfield (Hertfordshire), Hatf | 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
Save for laterRegister your CV04/06/2024 | Fulltime | Chicago, Newark (MO), Tulsa (T | 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 | Kaiserslautern, Cambridge, Dar | 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
Save for later04/06/2024 | Fulltime | Tulsa (Tulsa), Towson, 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 | Kaiserslautern, Cambridge, Dar | 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
Save for later04/06/2024 | Fulltime | Kaiserslautern, Cambridge, Dar | 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
Save for later04/06/2024 | Fulltime | Kaiserslautern, Cambridge, Dar | 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
Save for later04/06/2024 | Fulltime | Kaiserslautern, Cambridge, Dar | 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
Save for later04/06/2024 | Fulltime | Kaiserslautern, Cambridge, Dar | 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
Save for later04/06/2024 | Fulltime | Tulsa (Tulsa), Towson, 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
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