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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.
Anforderungen
- 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
Aufgaben
- 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
Ausbildung
- Master-Abschluss
Sprachen
- Englisch – verhandlungssicher
Tools & Technologien
- SAS
- R
- CDISC
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- CSL Vifor
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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.
Anforderungen
- 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
Aufgaben
- 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
Ausbildung
- Master-Abschluss
Sprachen
- Englisch – verhandlungssicher
Tools & Technologien
- SAS
- R
- CDISC
Über das Unternehmen
CSL Behring
Branche
Pharmaceuticals
Beschreibung
Das Unternehmen ist ein globaler Marktführer in der Biotherapeutik, der innovative Therapien für Patienten mit immunologischen, hämatologischen, kardiovaskulären und anderen Erkrankungen entwickelt.
Noch nicht perfekt?
- CSL Plasma
Principal Biostatistician(m/w/x)
Vollzeitnur vor OrtSeniorSchlieren - CSL Vifor
Associate Director, Biostatistics(m/w/x)
Vollzeitnur vor OrtSeniorGlattbrugg - Takeda Pharmaceuticals International AG
Manager, Site Start Up(m/w/x)
Vollzeitnur vor OrtSeniorZürich - CSL Behring
Senior Director Global Clinical Program Lead Cardiovascular & Renal(m/w/x)
Vollzeitnur vor OrtSeniorGlattbrugg - DeepMind
Senior Data Scientist(m/w/x)
Vollzeitnur vor OrtSeniorZürich