22/05/2024 | Fulltime | Kaiserslautern | BioNTech SEOn regulatory submissions, including developing ISE/ISS packages Excellent knowledge and experience of clinical development, study designs, advanced statistical methods (adaptive design and/or Bayesian is a plus), regulatory guidelines (ICH, FDA, EMA) Excellent knowledge of statistical analysis software (SAS
Save for later22/05/2024 | Fulltime | Kaiserslautern | BioNTech SEOn regulatory submissions, including developing ISE/ISS packages Excellent knowledge and experience of clinical development, study designs, advanced statistical methods (adaptive design and/or Bayesian is a plus), regulatory guidelines (ICH, FDA, EMA) Excellent knowledge of statistical analysis software (SAS
Save for later22/05/2024 | Fulltime | Kaiserslautern | BioNTech SEOn regulatory submissions, including developing ISE/ISS packages Excellent knowledge and experience of clinical development, study designs, advanced statistical methods (adaptive design and/or Bayesian is a plus), regulatory guidelines (ICH, FDA, EMA) Excellent knowledge of statistical analysis software (SAS
Save for later22/05/2024 | Fulltime | Kaiserslautern | BioNTech SEOn regulatory submissions, including developing ISE/ISS packages Excellent knowledge and experience of clinical development, study designs, advanced statistical methods (adaptive design and/or Bayesian is a plus), regulatory guidelines (ICH, FDA, EMA) Excellent knowledge of statistical analysis software (SAS
Save for later22/05/2024 | Fulltime | Kaiserslautern | BioNTech SEOn regulatory submissions, including developing ISE/ISS packages Excellent knowledge and experience of clinical development, study designs, advanced statistical methods (adaptive design and/or Bayesian is a plus), regulatory guidelines (ICH, FDA, EMA) Excellent knowledge of statistical analysis software (SAS
Save for later22/05/2024 | Fulltime | Kaiserslautern | BioNTech SEOn regulatory submissions, including developing ISE/ISS packages Excellent knowledge and experience of clinical development, study designs, advanced statistical methods (adaptive design and/or Bayesian is a plus), regulatory guidelines (ICH, FDA, EMA) Excellent knowledge of statistical analysis software (SAS
Save for later22/05/2024 | Fulltime | Kaiserslautern | BioNTech SEOn regulatory submissions, including developing ISE/ISS packages Excellent knowledge and experience of clinical development, study designs, advanced statistical methods (adaptive design and/or Bayesian is a plus), regulatory guidelines (ICH, FDA, EMA) Excellent knowledge of statistical analysis software (SAS
Save for later22/05/2024 | Fulltime | Kaiserslautern | BioNTech SEOn regulatory submissions, including developing ISE/ISS packages Excellent knowledge and experience of clinical development, study designs, advanced statistical methods (adaptive design and/or Bayesian is a plus), regulatory guidelines (ICH, FDA, EMA) Excellent knowledge of statistical analysis software (SAS
Save for later22/05/2024 | Fulltime | Kaiserslautern | BioNTech SEOn regulatory submissions, including developing ISE/ISS packages Excellent knowledge and experience of clinical development, study designs, advanced statistical methods (adaptive design and/or Bayesian is a plus), regulatory guidelines (ICH, FDA, EMA) Excellent knowledge of statistical analysis software (SAS
Save for later22/05/2024 | Fulltime | | Germany | CV-Library | £60,426 - £73,375 / Year The project lifecycle. Qualifications Bachelor's degree in Electrical Engineering or a related field. Proven experience in electrical engineering within the data centre or critical infrastructure sector. Proficiency in AutoCAD, Revit, or similar design software. Strong understanding of electrical systems
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