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Senior Biostatistician(m/w/x)
Description
In this role, you will drive the statistical strategy for clinical trials, ensuring high-quality data analysis and regulatory compliance while overseeing critical deliverables from start to finish.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •PhD or MS in Biostatistics, Statistics, or related field
- •PhD with 3 years drug development experience or comparable
- •MS with 6 years drug development experience
- •Advanced knowledge of clinical development statistical methodologies
- •Effective collaboration and leadership in matrix environments
- •Strong interpersonal and English communication skills
- •Proficiency in SAS and/or R
- •Familiarity with relevant regulatory guidance documents
- •Knowledge of CDISC, statistical programming, or data standards
- •Biostatistics and Statistical Programming Operations knowledge
Education
Tasks
- •Lead statistical contributions for clinical development programs
- •Implement statistical strategies for clinical trials
- •Apply methodologies to study design and analysis
- •Support data collection and submission preparation
- •Ensure quality of Statistical Analysis Plans
- •Manage interactions with regulatory authorities
- •Interpret analysis results for accurate reporting
- •Oversee outsourced statistical activities and CRO deliverables
- •Manage preparation of TFLs and CDISC packages
- •Contribute to continuous improvement and process standards
Tools & Technologies
Languages
English – Business Fluent
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Senior Biostatistician(m/w/x)
The AI Job Search Engine
Description
In this role, you will drive the statistical strategy for clinical trials, ensuring high-quality data analysis and regulatory compliance while overseeing critical deliverables from start to finish.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •PhD or MS in Biostatistics, Statistics, or related field
- •PhD with 3 years drug development experience or comparable
- •MS with 6 years drug development experience
- •Advanced knowledge of clinical development statistical methodologies
- •Effective collaboration and leadership in matrix environments
- •Strong interpersonal and English communication skills
- •Proficiency in SAS and/or R
- •Familiarity with relevant regulatory guidance documents
- •Knowledge of CDISC, statistical programming, or data standards
- •Biostatistics and Statistical Programming Operations knowledge
Education
Tasks
- •Lead statistical contributions for clinical development programs
- •Implement statistical strategies for clinical trials
- •Apply methodologies to study design and analysis
- •Support data collection and submission preparation
- •Ensure quality of Statistical Analysis Plans
- •Manage interactions with regulatory authorities
- •Interpret analysis results for accurate reporting
- •Oversee outsourced statistical activities and CRO deliverables
- •Manage preparation of TFLs and CDISC packages
- •Contribute to continuous improvement and process standards
Tools & Technologies
Languages
English – Business Fluent
About the Company
CSL Behring
Industry
Pharmaceuticals
Description
Das Unternehmen ist ein globaler Marktführer in der Biotherapeutik, der innovative Therapien für Patienten mit immunologischen, hämatologischen, kardiovaskulären und anderen Erkrankungen entwickelt.
- CSL Plasma
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Associate Director, Hematology(m/w/x)
Full-timeOn-siteSeniorSchlieren - Takeda
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