21/03/2024 | Fulltime | Cambridge | 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 | Cambridge | 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 | Cambridge | 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 | Cambridge | 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 | Cambridge | 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 | Cambridge | 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 | Cambridge | 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 | Cambridge | 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 | Cambridge | 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 | Cambridge | CV-Library | £27,900 - £36,300 / Year A degree in your subject, or a very closely related subject. Your standard of English will be very high, and knowledge of assessments in an education setting is key. You will have spent some time in the classroom as a teacher and may even have a knowledge of International education. Qualifications
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