04/06/2024 | Fulltime | Cambridge, Hanau, Wiesbaden, L | BioNTech SEAnd submission experience is preferred. Project management experience. Strong understanding of FDA, EMA, ICH, and global regulations and guidelines. Solid knowledge and experience of industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards. BioNTech
Save for later04/06/2024 | Fulltime | Mannheim, Aschaffenburg, Worms | BioNTech SEAnd submission experience is preferred. Project management experience. Strong understanding of FDA, EMA, ICH, and global regulations and guidelines. Solid knowledge and experience of industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards. BioNTech
Save for later29/05/2024 | Fulltime | Cambridge, Hanau, Ludwigshafen | BioNTech SEAll operational activities required to manage the lifecycle of biomarker samples in global phase I-IV clinical trials Support biomarker operational deliverables to be achieved in time and quality (including ICH/GCP regulations) Management of biomarker samples in projects with high complexity
Save for later29/05/2024 | Fulltime | Aschaffenburg, Worms, Offenbac | BioNTech SEAll operational activities required to manage the lifecycle of biomarker samples in global phase I-IV clinical trials Support biomarker operational deliverables to be achieved in time and quality (including ICH/GCP regulations) Management of biomarker samples in projects with high complexity
Save for later29/05/2024 | Fulltime | Wiesbaden, Ludwigshafen am Rhe | BioNTech SEAll operational activities required to manage the lifecycle of biomarker samples in global phase I-IV clinical trials Support biomarker operational deliverables to be achieved in time and quality (including ICH/GCP regulations) Management of biomarker samples in projects with high complexity
Save for later29/05/2024 | Fulltime | Hanau, Cambridge, Mainz, Wiesb | 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
Save for later29/05/2024 | Fulltime | Aschaffenburg, Offenbach am Ma | 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
Save for later29/05/2024 | Fulltime | Mannheim, Worms, Offenbach am | BioNTech SEAll operational activities required to manage the lifecycle of biomarker samples in global phase I-IV clinical trials Support biomarker operational deliverables to be achieved in time and quality (including ICH/GCP regulations) Management of biomarker samples in projects with high complexity
Save for later29/05/2024 | Fulltime | Worms, Poznań, Offenbach am Ma | BioNTech SEAll operational activities required to manage the lifecycle of biomarker samples in global phase I-IV clinical trials Support biomarker operational deliverables to be achieved in time and quality (including ICH/GCP regulations) Management of biomarker samples in projects with high complexity
Save for later29/05/2024 | Fulltime | Darmstadt, Kaiserslautern, Fra | 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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