CSL Vifor
Associate Director, Biostatistics(m/w/x)
Full-timeOn-siteSenior
Glattbrugg
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CSCSL Behring
Associate Director, Statistical Programming(m/w/x)
Glattbrugg
Full-timeOn-siteSenior
AI/ML
Nejo AI Summary
Leading statistical programming for biotherapeutics development across immunology and hematology. Advanced CDISC standards knowledge required. Well-being support and flexible work arrangements.
Requirements
- BSc in Computer Science, Mathematics, Statistics or related area
- Other degrees and certifications with commensurate programming experience
- Comprehensive understanding of clinical/statistical programming processes and standards
- Advanced knowledge in CDISC standards (CDASH, SDTM, ADaM)
- Ability to work independently or in a team, manage timelines
- Experience in cross-functional, multicultural, international clinical trial teams
- Interest and/or experience expanding beyond SAS
- Experience in/passion for automatization of routine programming tasks
- Broad knowledge of clinical development and processes
- Strong interpersonal and communication skills (verbal/written English)
- Ability to collaboratively work in matrix environment
- Solutions oriented mindset
- Fluency in technical requirements for CDISC datasets and DDT files
- Presentations of programming techniques at professional conferences (plus)
Tasks
- Lead development and maintenance of CSL statistical programming capabilities
- Collaborate with Director, Statistical Programming to manage tasks to completion
- Work with Statisticians to ensure deliverables meet CSL standards
- Manage Therapeutic Areas or programs, ensuring timely and high-quality work
- Assess upcoming activities and resource needs for project planning
- Oversee CRO delivery or manage in-house programming of clinical trial data
- Design and implement complex specifications and programs for clinical data
- Coordinate exploratory analyses and responses to regulatory requests
- Mentor and provide feedback to programmers on assigned projects
- Ensure compliance with programming processes and strategies
- Test and implement advanced programming methods and tools
- Drive automation of delivery, including AI integration
Work Experience
- 9 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Tools & Technologies
- SAS Software
- SAS Macros
- CDISC standards
- CDASH
- SDTM
- ADaM
Benefits
Mental Health Support
- Well-being support
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of CSL Behring and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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CSCSL Behring
Associate Director, Statistical Programming(m/w/x)
Glattbrugg
Full-timeOn-siteSenior
AI/ML
Nejo AI Summary
Leading statistical programming for biotherapeutics development across immunology and hematology. Advanced CDISC standards knowledge required. Well-being support and flexible work arrangements.
Requirements
- BSc in Computer Science, Mathematics, Statistics or related area
- Other degrees and certifications with commensurate programming experience
- Comprehensive understanding of clinical/statistical programming processes and standards
- Advanced knowledge in CDISC standards (CDASH, SDTM, ADaM)
- Ability to work independently or in a team, manage timelines
- Experience in cross-functional, multicultural, international clinical trial teams
- Interest and/or experience expanding beyond SAS
- Experience in/passion for automatization of routine programming tasks
- Broad knowledge of clinical development and processes
- Strong interpersonal and communication skills (verbal/written English)
- Ability to collaboratively work in matrix environment
- Solutions oriented mindset
- Fluency in technical requirements for CDISC datasets and DDT files
- Presentations of programming techniques at professional conferences (plus)
Tasks
- Lead development and maintenance of CSL statistical programming capabilities
- Collaborate with Director, Statistical Programming to manage tasks to completion
- Work with Statisticians to ensure deliverables meet CSL standards
- Manage Therapeutic Areas or programs, ensuring timely and high-quality work
- Assess upcoming activities and resource needs for project planning
- Oversee CRO delivery or manage in-house programming of clinical trial data
- Design and implement complex specifications and programs for clinical data
- Coordinate exploratory analyses and responses to regulatory requests
- Mentor and provide feedback to programmers on assigned projects
- Ensure compliance with programming processes and strategies
- Test and implement advanced programming methods and tools
- Drive automation of delivery, including AI integration
Work Experience
- 9 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Tools & Technologies
- SAS Software
- SAS Macros
- CDISC standards
- CDASH
- SDTM
- ADaM
Benefits
Mental Health Support
- Well-being support
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of CSL Behring and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
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 Vifor
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Biometrician/Epidemiologist/Statistics/SAS Programmer/Data Analyst(m/w/x)
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Full-timeOn-siteExperiencedBülach