22/05/2024 | Fulltime | Wiesbaden | 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 | Aschaffenburg | 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 | Offenbach am Main | 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 | Mainz | 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 | Worms | 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 | Wiesbaden | 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 | Mainz | 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 | Mainz | 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 | Ludwigshafen am Rhein | 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 later06/10/2022 | Fulltime | Walnut (CA) | Vercel | £90,000 - £120,000 Reliability across multiple microservices and have hands-on knowledge of the configuration of state of the art monitoring and logging tools. Responsibilities - About the role In this role you will be tasked with the overall development and implementation of front and back-end software applications. Your
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