06.06.24 | Vollzeit | Kaiserslautern | 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
Später ansehen06.06.24 | Vollzeit | Offenbach am Main | 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
Später ansehen06.06.24 | Vollzeit | Offenbach am Main | BioNTech SEAnd work closely with Clinical Data Manager to ensure data quality standards are met Open for hire at one of the following locations - Mainz K1. - Job ID 5210 PhD or Masters in (Bio)Statistics, Mathematics or equivalent Minimum 10 years (13 years for masters) in the pharmaceutical industry and/or CRO
Später ansehen06.06.24 | Vollzeit | Offenbach am Main | BioNTech SEAnd work closely with Clinical Data Manager to ensure data quality standards are met Open for hire at one of the following locations - Mainz K1. - Job ID 5210 PhD or Masters in (Bio)Statistics, Mathematics or equivalent Minimum 10 years (13 years for masters) in the pharmaceutical industry and/or CRO
Später ansehen06.06.24 | Vollzeit | Ludwigshafen am Rhein | BioNTech SEUnited, innovative, passionate. Get in touch with us if you are looking to be a part of creating hope for a healthy future in many people's lives. (Senior) Manager* Statistical Programming Work collaboratively with Clinical Development team or CRO to meet project deliverables and timelines
Später ansehen06.06.24 | Vollzeit | Kaiserslautern | 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
Später ansehen06.06.24 | Vollzeit | Kaiserslautern | 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
Später ansehen06.06.24 | Vollzeit | Kaiserslautern | 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
Später ansehen06.06.24 | Vollzeit | Kaiserslautern | BioNTech SEUnited, innovative, passionate. Get in touch with us if you are looking to be a part of creating hope for a healthy future in many people's lives. (Senior) Manager* Statistical Programming Work collaboratively with Clinical Development team or CRO to meet project deliverables and timelines
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