21/03/2024 | Fulltime | Offenbach am Main | BioNTech SETo the integrated development plan, clinical development plan, and to regulatory study- or program-related documents such as clinical trial protocols, and -reports, investigator brochures, briefing documents, and market authorization applications Contributes to the execution of the translational and biomarker
Save for later21/03/2024 | Fulltime | Aschaffenburg | BioNTech SETo the integrated development plan, clinical development plan, and to regulatory study- or program-related documents such as clinical trial protocols, and -reports, investigator brochures, briefing documents, and market authorization applications Contributes to the execution of the translational and biomarker
Save for later21/03/2024 | Fulltime | Kaiserslautern | BioNTech SETo the integrated development plan, clinical development plan, and to regulatory study- or program-related documents such as clinical trial protocols, and -reports, investigator brochures, briefing documents, and market authorization applications Contributes to the execution of the translational and biomarker
Save for later21/03/2024 | Fulltime | Rüsselsheim | BioNTech SETo the integrated development plan, clinical development plan, and to regulatory study- or program-related documents such as clinical trial protocols, and -reports, investigator brochures, briefing documents, and market authorization applications Contributes to the execution of the translational and biomarker
Save for later21/03/2024 | Fulltime | Aschaffenburg | BioNTech SETo the integrated development plan, clinical development plan, and to regulatory study- or program-related documents such as clinical trial protocols, and -reports, investigator brochures, briefing documents, and market authorization applications Contributes to the execution of the translational and biomarker
Save for later21/03/2024 | Fulltime | Mainz | BioNTech SETo the integrated development plan, clinical development plan, and to regulatory study- or program-related documents such as clinical trial protocols, and -reports, investigator brochures, briefing documents, and market authorization applications Contributes to the execution of the translational and biomarker
Save for later21/03/2024 | Fulltime | Wiesbaden | BioNTech SETo the integrated development plan, clinical development plan, and to regulatory study- or program-related documents such as clinical trial protocols, and -reports, investigator brochures, briefing documents, and market authorization applications Contributes to the execution of the translational and biomarker
Save for later21/03/2024 | Fulltime | Kaiserslautern | BioNTech SETo the integrated development plan, clinical development plan, and to regulatory study- or program-related documents such as clinical trial protocols, and -reports, investigator brochures, briefing documents, and market authorization applications Contributes to the execution of the translational and biomarker
Save for later21/03/2024 | Fulltime | Kaiserslautern | BioNTech SETo the integrated development plan, clinical development plan, and to regulatory study- or program-related documents such as clinical trial protocols, and -reports, investigator brochures, briefing documents, and market authorization applications Contributes to the execution of the translational and biomarker
Save for later15/03/2024 | Fulltime | Huntingdon | CV-Library | £35,000 / Year Of the operation. - Auditing HSE performance v's HSE KPI's along with correct safety behaviours, taking remedial action as required. - With SMT, review accident/ near miss and hazard trends. - Ensures all accidents are investigated by competent investigators, ensuring root causes have been identified, ensuring
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