18/06/2024 | Fulltime | Cambridge | MundipharmaPartners, and our employees. The Global Regulatory & Operations Senior Director is responsible for overseeing Regulatory Affairs (RA) Operations, including Global regulatory efforts, Regulatory systems management, vendor coordination, process optimization, and data analytics. They ensure Mundipharma team
Save for later17/06/2024 | Fulltime | Cambridge | MundipharmaPartners, and our employees. The Global Regulatory & Operations Senior Director is responsible for overseeing Regulatory Affairs (RA) Operations, including Global regulatory efforts, Regulatory systems management, vendor coordination, process optimization, and data analytics. They ensure Mundipharma team
Save for later17/06/2024 | Fulltime | Cambridge | MundipharmaOperations Senior Director is responsible for overseeing Regulatory Affairs (RA) Operations, including Global regulatory efforts, Regulatory systems management, vendor coordination, process optimization, and data analytics. They ensure Mundipharma team members deliver Global RA initiatives
Save for later17/06/2024 | Fulltime | Cambridge | MundipharmaSenior Director is responsible for overseeing Regulatory Affairs (RA) Operations, including Global regulatory efforts, Regulatory systems management, vendor coordination, process optimization, and data analytics. They ensure Mundipharma team members deliver Global RA initiatives in designated
Save for later17/06/2024 | Fulltime | Cambridge | MundipharmaPartners, and our employees. The Global Regulatory & Operations Senior Director is responsible for overseeing Regulatory Affairs (RA) Operations, including Global regulatory efforts, Regulatory systems management, vendor coordination, process optimization, and data analytics. They ensure Mundipharma team
Save for later17/06/2024 | Fulltime | Cambridge | MundipharmaPartners, and our employees. The Global Regulatory & Operations Senior Director is responsible for overseeing Regulatory Affairs (RA) Operations, including Global regulatory efforts, Regulatory systems management, vendor coordination, process optimization, and data analytics. They ensure Mundipharma team
Save for later06/06/2024 | Fulltime | Hanau | BioNTech SESubmissions and managing people Oncology or Infectious Disease therapeutic areas and submission experience is preferred Strong leadership and project management skills as well as proficiency in English (spoken and written) BioNTech is committed to the wellbeing of our team members and offers a variety
Save for later06/06/2024 | Fulltime | Kaiserslautern | BioNTech SETo database requirements and work closely with Clinical Data Manager to ensure data quality standards are met PhD or Masters in (Bio)Statistics, Mathematics or equivalent Minimum 5 years (8 years for masters) in the pharmaceutical industry and/or CRO At least 3 years of work/leadership experience, overseeing
Save for later06/06/2024 | Fulltime | Cambridge | BioNTech SESubmissions and managing people Oncology or Infectious Disease therapeutic areas and submission experience is preferred Strong leadership and project management skills as well as proficiency in English (spoken and written) BioNTech is committed to the wellbeing of our team members and offers a variety
Save for later06/06/2024 | Fulltime | Kaiserslautern | BioNTech SEFor statistical data analysis and reporting Independently perform or oversee the production and/or validation of programming deliverables (e.g., analysis datasets, tables, listings) for study reports and integrated summaries Anticipate resource needs and works with management to ensure adequate long-term resource
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