Novartis Pharma AG
Senior Principal Statistical Programmer(m/w/x)
Full-timeRemoteManagement
Basel
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NONovartis Pharma AG
Senior Principal Statistical Programmer(m/w/x)
Basel
Full-timeWith Home OfficeManagement
Nejo AI Summary
Statistical programming for multiple clinical studies, coordinating internal/external teams at a patient-care focused pharma company. Expert SAS experience with advanced MACRO development skills and clinical trials programming experience required. Workplace support for recruitment and essential functions.
Requirements
- Degree in statistics, computer science, mathematics, life sciences or equivalent
- Programming experience in clinical trials or pharmaceutical industry
- Expert SAS experience and advanced MACRO development skills
- Experience in statistical analysis plans or technical programming specifications
- Advanced knowledge of CDISC data structures and standard programs
- Understanding of regulatory requirements like GCP and study procedures
- Proven communications, negotiation, and global influence skills
- Experience as Lead Programmer and team coordination skills
- Skills in data analysis, reporting, and cross-functional teams
Tasks
- Lead statistical programming for multiple clinical studies
- Manage programming for medium to large-scale projects
- Coordinate internal and external programming teams
- Propose strategies and make key programming decisions
- Supervise and advise local programming associates
- Collaborate with cross-functional teams on project status
- Review eCRF and standardize data structures
- Ensure compliance with CDISC and industry standards
- Develop and influence detailed programming specifications
- Implement expert statistical programming solutions
- Validate datasets for regulatory submissions and reports
- Maintain audit readiness for all programming deliverables
- Master SAS and advanced industry software requirements
- Manage relationships with external vendors and associates
- Lead process improvement and non-clinical project initiatives
Education
- Bachelor's degree
Languages
- English – Business Fluent
Tools & Technologies
- SAS
- MACROs
- CDISC
Benefits
Other Benefits
- Reasonable accommodation for recruitment
- Reasonable accommodation for essential functions
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Novartis Pharma AG 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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NONovartis Pharma AG
Senior Principal Statistical Programmer(m/w/x)
Basel
Full-timeWith Home OfficeManagement
Nejo AI Summary
Statistical programming for multiple clinical studies, coordinating internal/external teams at a patient-care focused pharma company. Expert SAS experience with advanced MACRO development skills and clinical trials programming experience required. Workplace support for recruitment and essential functions.
Requirements
- Degree in statistics, computer science, mathematics, life sciences or equivalent
- Programming experience in clinical trials or pharmaceutical industry
- Expert SAS experience and advanced MACRO development skills
- Experience in statistical analysis plans or technical programming specifications
- Advanced knowledge of CDISC data structures and standard programs
- Understanding of regulatory requirements like GCP and study procedures
- Proven communications, negotiation, and global influence skills
- Experience as Lead Programmer and team coordination skills
- Skills in data analysis, reporting, and cross-functional teams
Tasks
- Lead statistical programming for multiple clinical studies
- Manage programming for medium to large-scale projects
- Coordinate internal and external programming teams
- Propose strategies and make key programming decisions
- Supervise and advise local programming associates
- Collaborate with cross-functional teams on project status
- Review eCRF and standardize data structures
- Ensure compliance with CDISC and industry standards
- Develop and influence detailed programming specifications
- Implement expert statistical programming solutions
- Validate datasets for regulatory submissions and reports
- Maintain audit readiness for all programming deliverables
- Master SAS and advanced industry software requirements
- Manage relationships with external vendors and associates
- Lead process improvement and non-clinical project initiatives
Education
- Bachelor's degree
Languages
- English – Business Fluent
Tools & Technologies
- SAS
- MACROs
- CDISC
Benefits
Other Benefits
- Reasonable accommodation for recruitment
- Reasonable accommodation for essential functions
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Novartis Pharma AG 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.
About the Company
Novartis Pharma AG
Industry
Pharmaceuticals
Description
Das Unternehmen setzt sich für Vielfalt, Chancengleichheit und Inklusion ein und fördert innovative Lösungen zur Verbesserung der Patientenversorgung.
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