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Principal Quantitative Scientist(m/w/x)
Leading RWD study design and developing methodologies for clinical trials and evidence generation. 5-7 years statistical analysis experience and extensive RWD study design knowledge in regulated environments required. Direct impact on global health outcomes through RWD innovation.
Requirements
- Master’s degree or PhD in natural sciences with a focus on statistics
- At least 5–7 years (Master’s) or 3–5 years (PhD) of relevant experience in statistical analysis and epidemiology
- Very good knowledge of statistical programming languages (e.g., R, SAS) and sound knowledge of data management
- Extensive knowledge of Real World Data study design and confidence in regulated/validated environment
- Excellent communication skills and strong stakeholder management abilities
- International, strategic, and goal-oriented mindset with high capacity for learning
- Fluency in both German and English, written and spoken
Tasks
- Lead and design RWD studies
- Create precise study designs and Statistical Analysis Plans
- Coordinate consolidation of complex data
- Develop innovative RWD methodologies for clinical trials
- Identify opportunities for RWD in evidence generation
- Process and visualize large-scale RWD using programming tools
- Collaborate with internal stakeholders and external partners
- Publish high-quality study results at international congresses
Work Experience
- 3 - 5 years
Education
- Master's degree
Languages
- German – Business Fluent
- English – Business Fluent
Tools & Technologies
- R
- SAS
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Principal Quantitative Scientist(m/w/x)
Leading RWD study design and developing methodologies for clinical trials and evidence generation. 5-7 years statistical analysis experience and extensive RWD study design knowledge in regulated environments required. Direct impact on global health outcomes through RWD innovation.
Requirements
- Master’s degree or PhD in natural sciences with a focus on statistics
- At least 5–7 years (Master’s) or 3–5 years (PhD) of relevant experience in statistical analysis and epidemiology
- Very good knowledge of statistical programming languages (e.g., R, SAS) and sound knowledge of data management
- Extensive knowledge of Real World Data study design and confidence in regulated/validated environment
- Excellent communication skills and strong stakeholder management abilities
- International, strategic, and goal-oriented mindset with high capacity for learning
- Fluency in both German and English, written and spoken
Tasks
- Lead and design RWD studies
- Create precise study designs and Statistical Analysis Plans
- Coordinate consolidation of complex data
- Develop innovative RWD methodologies for clinical trials
- Identify opportunities for RWD in evidence generation
- Process and visualize large-scale RWD using programming tools
- Collaborate with internal stakeholders and external partners
- Publish high-quality study results at international congresses
Work Experience
- 3 - 5 years
Education
- Master's degree
Languages
- German – Business Fluent
- English – Business Fluent
Tools & Technologies
- R
- SAS
About the Company
Roche Diagnostics GmbH
Industry
Healthcare
Description
Das Unternehmen setzt sich dafür ein, Krankheiten zu verhindern, zu stoppen und zu heilen, und gewährleistet den Zugang zur Gesundheitsversorgung.
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