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Senior Biostatistician(m/w/x)
Leading statistical contributions for clinical development programs for immunological, hematological, cardiovascular therapies. PhD with 3 years or MS with 6 years drug development experience required. Impact on global clinical development, leadership in matrix environments.
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
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
Education
- Master's degree
Languages
- English – Business Fluent
Tools & Technologies
- SAS
- R
- CDISC
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Senior Biostatistician(m/w/x)
Leading statistical contributions for clinical development programs for immunological, hematological, cardiovascular therapies. PhD with 3 years or MS with 6 years drug development experience required. Impact on global clinical development, leadership in matrix environments.
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
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
Education
- Master's degree
Languages
- English – Business Fluent
Tools & Technologies
- SAS
- R
- CDISC
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.
Not a perfect match?
- CSL Plasma
Principal Biostatistician(m/w/x)
Full-timeOn-siteSeniorSchlieren - CSL Vifor
Associate Director, Biostatistics(m/w/x)
Full-timeOn-siteSeniorGlattbrugg - Takeda Pharmaceuticals International AG
Manager, Site Start Up(m/w/x)
Full-timeOn-siteSeniorZürich - CSL Behring
Senior Director Global Clinical Program Lead Cardiovascular & Renal(m/w/x)
Full-timeOn-siteSeniorGlattbrugg - DeepMind
Senior Data Scientist(m/w/x)
Full-timeOn-siteSeniorZürich