24.04.24 | Vollzeit | Mainz | BioNTech SEAnd the preparation of associated responses Oversee outsourced statistical CRO activities and deliverables ensuring highest quality and in a timely manner Support and participate in the development of departmental strategies Provide guidance to Statistical Programmers on SDTM/ADaM and TLFs specifications development
Später ansehen17.04.24 | Vollzeit | Ingelheim am Rhein | JobLeads GmbH | 100.000 € - 125.000 € Tools and techniques. - Regulatory Knowledge An understanding of global regulatory requirements, guidelines, and procedures. This includes knowledge of the regulatory landscape in different regions and the ability to interpret and apply regulatory guidance to various situations. - Strategic Thinking
Später ansehen09.04.24 | Vollzeit | Offenbach am Main | BioNTech SECross-functional team with members from other disciplines Provide statistical guidance into clinical development plans, clinical study protocols, clinical study reports, regulatory submission documents, and publications ensuring accurate deliverables Perform and/or verify sample size calculations Lead
Später ansehen09.04.24 | Vollzeit | Kaiserslautern | BioNTech SECross-functional team with members from other disciplines Provide statistical guidance into clinical development plans, clinical study protocols, clinical study reports, regulatory submission documents, and publications ensuring accurate deliverables Perform and/or verify sample size calculations Lead
Später ansehen09.04.24 | Vollzeit | Darmstadt | BioNTech SECross-functional team with members from other disciplines Provide statistical guidance into clinical development plans, clinical study protocols, clinical study reports, regulatory submission documents, and publications ensuring accurate deliverables Perform and/or verify sample size calculations Lead
Später ansehen09.04.24 | Vollzeit | Kaiserslautern | BioNTech SECross-functional team with members from other disciplines Provide statistical guidance into clinical development plans, clinical study protocols, clinical study reports, regulatory submission documents, and publications ensuring accurate deliverables Perform and/or verify sample size calculations Lead
Später ansehen09.04.24 | Vollzeit | Kaiserslautern | BioNTech SECross-functional team with members from other disciplines Provide statistical guidance into clinical development plans, clinical study protocols, clinical study reports, regulatory submission documents, and publications ensuring accurate deliverables Perform and/or verify sample size calculations Lead
Später ansehen09.04.24 | Vollzeit | Kaiserslautern | BioNTech SECross-functional team with members from other disciplines Provide statistical guidance into clinical development plans, clinical study protocols, clinical study reports, regulatory submission documents, and publications ensuring accurate deliverables Perform and/or verify sample size calculations Lead
Später ansehen09.04.24 | Vollzeit | Kaiserslautern | BioNTech SECross-functional team with members from other disciplines Provide statistical guidance into clinical development plans, clinical study protocols, clinical study reports, regulatory submission documents, and publications ensuring accurate deliverables Perform and/or verify sample size calculations Lead
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