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 | Kaiserslautern | 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 ansehen06.06.24 | Vollzeit | Kaiserslautern | BioNTech SETo database requirements and work closely with Clinical Data Manager to ensure data quality standards are met PhD or Masters in (Bio)Statistics, Mathematics or equivalent Minimum 5 years (8 years for masters) in the pharmaceutical industry and/or CRO At least 3 years of work/leadership experience, overseeing
Später ansehen06.06.24 | Vollzeit | Kaiserslautern | 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 | Kaiserslautern | 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 ansehen06.06.24 | Vollzeit | Kaiserslautern | 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 ansehen06.06.24 | Vollzeit | Kaiserslautern | 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 ansehen06.06.24 | Vollzeit | Kaiserslautern | BioNTech SETo database requirements and work closely with Clinical Data Manager to ensure data quality standards are met PhD or Masters in (Bio)Statistics, Mathematics or equivalent Minimum 5 years (8 years for masters) in the pharmaceutical industry and/or CRO At least 3 years of work/leadership experience, overseeing
Später ansehen06.06.24 | Vollzeit | Kaiserslautern | 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
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