06.06.24 | Vollzeit | Frankfurt am Main | BioNTech SEAnd reporting on clinical trials, including CDISC standards Solid understanding of the drug development process from early- to late-stage development and submission Expertise in the requirements and technology to support electronic submissions Strong project management skills Strong interpersonal skills
Später ansehen06.06.24 | Vollzeit | Offenbach am Main | BioNTech SEAnd global regulations and industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards Expertise in the requirements and technology required to support electronic submissions Experience in leading submissions and managing people Oncology or Infectious
Später ansehen06.06.24 | Vollzeit | Worms | BioNTech SEAnd reporting on clinical trials, including CDISC standards Solid understanding of the drug development process from early- to late-stage development and submission Expertise in the requirements and technology to support electronic submissions Strong project management skills Strong interpersonal skills
Später ansehen06.06.24 | Vollzeit | Offenbach am Main | BioNTech SEAnd reporting on clinical trials, including CDISC standards Solid understanding of the drug development process from early- to late-stage development and submission Expertise in the requirements and technology to support electronic submissions Strong project management skills Strong interpersonal skills
Später ansehen06.06.24 | Vollzeit | Kaiserslautern | BioNTech SEAnd global regulations and industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards Expertise in the requirements and technology required to support electronic submissions Experience in leading submissions and managing people Oncology or Infectious
Später ansehen06.06.24 | Vollzeit | Darmstadt | BioNTech SEAnd global regulations and industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards Expertise in the requirements and technology required to support electronic submissions Experience in leading submissions and managing people Oncology or Infectious
Später ansehen06.06.24 | Vollzeit | Mannheim | BioNTech SEAnd reporting on clinical trials, including CDISC standards Solid understanding of the drug development process from early- to late-stage development and submission Expertise in the requirements and technology to support electronic submissions Strong project management skills Strong interpersonal skills
Später ansehen06.06.24 | Vollzeit | Mainz | BioNTech SEAnd global regulations and industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards Expertise in the requirements and technology required to support electronic submissions Experience in leading submissions and managing people Oncology or Infectious
Später ansehen06.06.24 | Vollzeit | Mainz | BioNTech SEAnd reporting on clinical trials, including CDISC standards Solid understanding of the drug development process from early- to late-stage development and submission Expertise in the requirements and technology to support electronic submissions Strong project management skills Strong interpersonal skills
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