05.06.24 | Vollzeit | Ludwigshafen am Rhein | AbbVie Deutschland GmbH & Co. KGcompliance of IMP pharmaceutical drug and drug - device combination products with worldwide quality and regulatory requirements and IMPD - CTA applications Establish and regularly evaluate quality and key performance indicators, forwarding data for management reviews and communication to business partners
Später ansehen29.05.24 | Vollzeit | 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
Später ansehen29.05.24 | Vollzeit | 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
Später ansehen29.05.24 | Vollzeit | Kaiserslautern | BioNTech SEOperational activities required to 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
Später ansehen29.05.24 | Vollzeit | 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
Später ansehen29.05.24 | Vollzeit | Kaiserslautern | BioNTech SEOperational activities required to 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
Später ansehen29.05.24 | Vollzeit | 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
Später ansehen29.05.24 | Vollzeit | 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
Später ansehen29.05.24 | Vollzeit | Kaiserslautern | BioNTech SEOperational activities required to 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
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