04/06/2024 | Fulltime | Mannheim | 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 | Mainz | 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 | Hanau | 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 | Wiesbaden | 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 | 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
Save for later04/06/2024 | Fulltime | Darmstadt | 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 | Newark (AR) | BioNTech SEAreas and submission experience is preferred Strong interpersonal skills in addition to exceptional English written and oral communication skills, combined with the need to work closely with CROs, investigators, consultants, and team members across functions Project management experience and strong
Save for later04/06/2024 | Fulltime | Newark (DE) | BioNTech SEAreas and submission experience is preferred Strong interpersonal skills in addition to exceptional English written and oral communication skills, combined with the need to work closely with CROs, investigators, consultants, and team members across functions Project management experience and strong
Save for later04/06/2024 | Fulltime | Newark (OH) | BioNTech SEAreas and submission experience is preferred Strong interpersonal skills in addition to exceptional English written and oral communication skills, combined with the need to work closely with CROs, investigators, consultants, and team members across functions Project management experience and strong
Save for later04/06/2024 | 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
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