19/06/2024 | Fulltime | Huntingdon | MedMatchWith 20.6% Employer Contribution - 7.6 weeks of annual leave (inclusive of Bank Holidays) - Indemnity cover provided - Enhanced parental leave benefits - Continued professional development time and study leave - Well-being support services including Employee Assistance Program and Wellbeing Advisors
Save for later18/06/2024 | Fulltime | Cambridge | PharmiwebReports and share findings. - Keep accurate and up-to-date laboratory records. - Perform other duties as assigned based on qualifications. - Act as a technical reviewer for other projects, contribute to development seminars, and stand in for senior staff as needed. Requirements - A degree in a relevant
Save for later13/06/2024 | Parttime | Cambridge | CV-LibraryFantastic Opportunity for a Hardware or Software Engineer to work in the Architecture & Technology Group at Arm's Headquarters in Cambridge! JOB OVERVIEW We are looking for a highly motivated individual to work on development and maintenance of the parts of the Arm Architecture relating to virtual
Save for laterRegister your CV03/06/2024 | Parttime | Cambridge | CV-LibraryAnd scalable, either through custom application development or using Industry standard tools & capabilities. In parallel, you will also be encouraged to contribute to different parts of our existing technical infrastructure, including managing Databases, ETLs, and reporting pipelines! Responsibilities Define
Save for laterRegister your CV06/06/2024 | Fulltime | Kaiserslautern | BioNTech SEAccountable for all statistical aspects Work as part of a collaborative, cross-functional team with members from other disciplines Provide statistical input into clinical development plans, clinical study protocols, clinical study reports, regulatory submission documents, and publications ensuring accurate
Save for later06/06/2024 | Fulltime | Kaiserslautern | BioNTech SEFrom Clinical Development, Clinical Operations, Regulatory Affairs, and others to meet project deliverables and timelines for statistical data analysis and reporting Guide and collaborate with internal Global Biometric Sciences (GBS) project leads and CRO staff to ensure alignment with established data
Save for later06/06/2024 | Fulltime | Kaiserslautern | BioNTech SEFrom Clinical Development, Clinical Operations, Regulatory Affairs, and others to meet project deliverables and timelines for statistical data analysis and reporting Guide and collaborate with internal Global Biometric Sciences (GBS) project leads and CRO staff to ensure alignment with established data
Save for later06/06/2024 | Fulltime | Kaiserslautern | BioNTech SEAccountable for all statistical aspects Work as part of a collaborative, cross-functional team with members from other disciplines Provide statistical input into clinical development plans, clinical study protocols, clinical study reports, regulatory submission documents, and publications ensuring accurate
Save for later06/06/2024 | Fulltime | Kaiserslautern | BioNTech SEAccountable for all statistical aspects Work as part of a collaborative, cross-functional team with members from other disciplines Provide statistical input into clinical development plans, clinical study protocols, clinical study reports, regulatory submission documents, and publications ensuring accurate
Save for later06/06/2024 | Fulltime | Kaiserslautern | BioNTech SEAccountable for all statistical aspects Work as part of a collaborative, cross-functional team with members from other disciplines Provide statistical input into clinical development plans, clinical study protocols, clinical study reports, regulatory submission documents, and publications ensuring accurate
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