22/05/2024 | Fulltime | Kaiserslautern | BioNTech SEPublications Experience in leading to answer health authority questions (FDA, EMA) and leading in statistics on regulatory submissions, including developing ISE/ISS packages Excellent knowledge and experience of clinical development, study designs, advanced statistical methods (adaptive design and/or Bayesian
Save for later22/05/2024 | Fulltime | Kaiserslautern | BioNTech SEPublications Experience in leading to answer health authority questions (FDA, EMA) and leading in statistics on regulatory submissions, including developing ISE/ISS packages Excellent knowledge and experience of clinical development, study designs, advanced statistical methods (adaptive design and/or Bayesian
Save for later22/05/2024 | Fulltime | Kaiserslautern | BioNTech SEPublications Experience in leading to answer health authority questions (FDA, EMA) and leading in statistics on regulatory submissions, including developing ISE/ISS packages Excellent knowledge and experience of clinical development, study designs, advanced statistical methods (adaptive design and/or Bayesian
Save for later22/05/2024 | Fulltime | Kaiserslautern | BioNTech SEPublications Experience in leading to answer health authority questions (FDA, EMA) and leading in statistics on regulatory submissions, including developing ISE/ISS packages Excellent knowledge and experience of clinical development, study designs, advanced statistical methods (adaptive design and/or Bayesian
Save for later22/05/2024 | Fulltime | Kaiserslautern | BioNTech SEPublications Experience in leading to answer health authority questions (FDA, EMA) and leading in statistics on regulatory submissions, including developing ISE/ISS packages Excellent knowledge and experience of clinical development, study designs, advanced statistical methods (adaptive design and/or Bayesian
Save for later22/05/2024 | Fulltime | Kaiserslautern | BioNTech SEPublications Experience in leading to answer health authority questions (FDA, EMA) and leading in statistics on regulatory submissions, including developing ISE/ISS packages Excellent knowledge and experience of clinical development, study designs, advanced statistical methods (adaptive design and/or Bayesian
Save for later22/05/2024 | Fulltime | Kaiserslautern | BioNTech SEPublications Experience in leading to answer health authority questions (FDA, EMA) and leading in statistics on regulatory submissions, including developing ISE/ISS packages Excellent knowledge and experience of clinical development, study designs, advanced statistical methods (adaptive design and/or Bayesian
Save for later22/05/2024 | Fulltime | Kaiserslautern | BioNTech SEPublications Experience in leading to answer health authority questions (FDA, EMA) and leading in statistics on regulatory submissions, including developing ISE/ISS packages Excellent knowledge and experience of clinical development, study designs, advanced statistical methods (adaptive design and/or Bayesian
Save for later22/05/2024 | Fulltime | Kaiserslautern | BioNTech SEPublications Experience in leading to answer health authority questions (FDA, EMA) and leading in statistics on regulatory submissions, including developing ISE/ISS packages Excellent knowledge and experience of clinical development, study designs, advanced statistical methods (adaptive design and/or Bayesian
Save for later02/06/2024 | Fulltime | Bristol | Reemtsma Cigarettenfabriken GmbHEffectively manage and maintain strong external relationships with key partners and technology providers. - Stay abreast of the latest technological advancements relvant to our industry and categories and be the go to extert for this knowledge. - Work closely with portfolio, category, and markets to assess
Save for later