12/03/2024 | Fulltime | Rüsselsheim | BioNTech SETo manage the lifecycle of biomarker samples in global Phase I-IV clinical trials Ensure biomarker sample related collection, tracking, and storage in compliance with the Clinical Trial Protocol and Patient Informed Consent Management of cross-functional integration and execution of operational biomarker
Save for later12/03/2024 | Fulltime | Kaiserslautern | BioNTech SETo manage the lifecycle of biomarker samples in global Phase I-IV clinical trials Ensure biomarker sample related collection, tracking, and storage in compliance with the Clinical Trial Protocol and Patient Informed Consent Management of cross-functional integration and execution of operational biomarker
Save for later12/03/2024 | Fulltime | Kaiserslautern | BioNTech SETo manage the lifecycle of biomarker samples in global Phase I-IV clinical trials Ensure biomarker sample related collection, tracking, and storage in compliance with the Clinical Trial Protocol and Patient Informed Consent Management of cross-functional integration and execution of operational biomarker
Save for later26/02/2024 | Fulltime | Kaiserslautern | BioNTech SEResponsibilities of staff and is responsible for recruiting, developing, and retaining talent Provide guidance to Statistical Programmers on SDTM/ADaM and TLFs specifications development and programming Provide input to database requirements and work closely with Clinical Data Manager to ensure data quality
Save for later26/02/2024 | Fulltime | Kaiserslautern | BioNTech SEResponsibilities of staff and is responsible for recruiting, developing, and retaining talent Provide guidance to Statistical Programmers on SDTM/ADaM and TLFs specifications development and programming Provide input to database requirements and work closely with Clinical Data Manager to ensure data quality
Save for later26/02/2024 | Fulltime | Kaiserslautern | BioNTech SEResponsibilities of staff and is responsible for recruiting, developing, and retaining talent Provide guidance to Statistical Programmers on SDTM/ADaM and TLFs specifications development and programming Provide input to database requirements and work closely with Clinical Data Manager to ensure data quality
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