23.04.24 | Vollzeit | Kaiserslautern | AbbVie Deutschland GmbH & Co. KGThe Manager works independently in partnership with experts in multiple disciplines to advance medicines to our patients. This means Statistical planning, design, analysis, and reporting related to clinical studies and other scientific research studies, including review and development of relevant study
Später ansehen08.05.24 | Vollzeit | Raunheim | TipTopJob Germany | As well as considering the overall client IT operating model, processes, tools and automation, and collaborates closely with the Enterprise Architect, to create a number of solution scenarios or user stories which support the development of the rightfit solution or service for the customer. As a Service
Später ansehen09.04.24 | Vollzeit | 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
Später ansehen09.04.24 | Vollzeit | 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
Später ansehen09.04.24 | Vollzeit | 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
Später ansehen09.04.24 | Vollzeit | 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
Später ansehen09.04.24 | Vollzeit | 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
Später ansehen09.04.24 | Vollzeit | 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
Später ansehen09.04.24 | Vollzeit | 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
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