06/06/2024 | 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 SEAnd global regulations and industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards Expertise in the requirements and technology required to support electronic submissions Experience in leading submissions and managing people Oncology or Infectious
Save for later06/06/2024 | Fulltime | Offenbach am Main | BioNTech SEAnd global regulations and industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards Expertise in the requirements and technology required to support electronic submissions Experience in leading submissions and managing people Oncology or Infectious
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 | 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 | 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 | Kaiserslautern | BioNTech SEOf industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards Oncology or Infectious Disease therapeutic areas and submission experience is preferred Project management experience, detail-oriented, and strong organizational and communication skills
Save for later06/06/2024 | Fulltime | Mainz | BioNTech SEAnd global regulations and industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards Expertise in the requirements and technology required to support electronic submissions Experience in leading submissions and managing people Oncology or Infectious
Save for later06/06/2024 | Fulltime | Cambridge | BioNTech SEAnd reporting on clinical trials, including CDISC standards Solid understanding of the drug development process from early- to late-stage development and submission Expertise in the requirements and technology to support electronic submissions Strong project management skills Strong interpersonal skills
Save for later06/06/2024 | Fulltime | Worms | BioNTech SEAnd global regulations and industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards Expertise in the requirements and technology required to support electronic submissions Experience in leading submissions and managing people Oncology or Infectious
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