06.06.24 | Vollzeit | Kaiserslautern, Darmstadt, Lud | BioNTech SEHealth authority questions (FDA, EMA) and in leadings statistics on regulatory submissions, including developing ISE/ISS packages Good knowledge and experience of clinical development, study designs, advanced statistical methods (adaptive design and/or Bayesian is a plus), regulatory guidelines (ICH, FDA
Später ansehen06.06.24 | Vollzeit | Kaiserslautern, Poznań, Darmst | 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, Darmstadt, Lud | 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, Poznań, Darmst | 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, Darmstadt, Lud | BioNTech SEHealth authority questions (FDA, EMA) and in leadings statistics on regulatory submissions, including developing ISE/ISS packages Good knowledge and experience of clinical development, study designs, advanced statistical methods (adaptive design and/or Bayesian is a plus), regulatory guidelines (ICH, FDA
Später ansehen06.06.24 | Vollzeit | Kaiserslautern, Darmstadt, Lud | BioNTech SEHealth authority questions (FDA, EMA) and in leadings statistics on regulatory submissions, including developing ISE/ISS packages Good knowledge and experience of clinical development, study designs, advanced statistical methods (adaptive design and/or Bayesian is a plus), regulatory guidelines (ICH, FDA
Später ansehen06.06.24 | Vollzeit | Kaiserslautern, Darmstadt, Lud | 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, Darmstadt, Lud | BioNTech SEHealth authority questions (FDA, EMA) and in leadings statistics on regulatory submissions, including developing ISE/ISS packages Good knowledge and experience of clinical development, study designs, advanced statistical methods (adaptive design and/or Bayesian is a plus), regulatory guidelines (ICH, FDA
Später ansehen06.06.24 | Vollzeit | Kaiserslautern, Darmstadt, Lud | 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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