09.04.24 | Vollzeit | Wiesbaden | Tecan Software Competence Center GmbHSoftware Tester* Wiesbaden, Germany Your contribution In this versatile role, you will be responsible for further customer-specific developments and adaptations of our software product portfolio in the diagnostic area. You will be part of an experienced team of software developers and testers
Später ansehen08.04.24 | Vollzeit | Wiesbaden | CureVac Corporate Services GmbHBy enabling end users to work with digital products and services Provide technical assistance and troubleshooting for end user devices, applications, and network connectivity Develop practices and processes to efficiently install, configure, and maintain hardware, software, and peripherals for end users
Später ansehen09.04.24 | Vollzeit | 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
Später ansehen09.04.24 | Vollzeit | 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
Später ansehen09.04.24 | Vollzeit | 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
Später ansehen09.04.24 | Vollzeit | 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
Später ansehen09.04.24 | Vollzeit | 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
Später ansehen09.04.24 | Vollzeit | 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
Später ansehen09.04.24 | Vollzeit | 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
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