06.06.24 | Vollzeit | Ludwigshafen am Rhein | BioNTech SEGuide and collaborate with internal Global Biometric Sciences (GBS) project leads and CRO staff to ensure alignment with established data, analysis and quality standards Identify and evaluate programming metrics to judge department performance and evaluates existing processes and guidelines
Später ansehen06.06.24 | Vollzeit | Frankfurt am Main | BioNTech SEGRAPH, SQL Solid understanding of FDA, EMA, ICH and 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
Später ansehen06.06.24 | Vollzeit | Ludwigshafen am Rhein | BioNTech SEGuide and collaborate with internal Global Biometric Sciences (GBS) project leads and CRO staff to ensure alignment with established data, analysis and quality standards Identify and evaluate programming metrics to judge department performance and evaluates existing processes and guidelines
Später ansehen06.06.24 | Vollzeit | Mainz | BioNTech SEGuide and collaborate with internal Global Biometric Sciences (GBS) project leads and CRO staff to ensure alignment with established data, analysis and quality standards Identify and evaluate programming metrics to judge department performance and evaluates existing processes and guidelines
Später ansehen06.06.24 | Vollzeit | Ludwigshafen am Rhein | BioNTech SEGuide and collaborate with internal Global Biometric Sciences (GBS) project leads and CRO staff to ensure alignment with established data, analysis and quality standards Identify and evaluate programming metrics to judge department performance and evaluates existing processes and guidelines
Später ansehen06.06.24 | Vollzeit | Ludwigshafen am Rhein | BioNTech SEGRAPH, SQL Solid understanding of FDA, EMA, ICH and 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
Später ansehen06.06.24 | Vollzeit | Frankfurt am Main | BioNTech SEGRAPH, SQL Solid understanding of FDA, EMA, ICH and 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
Später ansehen06.06.24 | Vollzeit | Mannheim | BioNTech SEGuide and collaborate with internal Global Biometric Sciences (GBS) project leads and CRO staff to ensure alignment with established data, analysis and quality standards Identify and evaluate programming metrics to judge department performance and evaluates existing processes and guidelines
Später ansehen06.06.24 | Vollzeit | Worms | BioNTech SEIncluding scientific publications Experience in leading to health authority questions (FDA, EMA) and in leadings statistics on regulatory submissions, including developing ISE/ISS packages Very good knowledge and experience of clinical development, study designs, advanced statistical methods (adaptive
Später ansehenVerpassen Sie nie wieder einen passenden Job!
Alle Jobs für Play Leader in Worms Landkreis kostenlos abonnieren.