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Novartis Pharma AG
5d ago

Senior Principal Statistical Programmer(m/w/x)

Basel
Full-timeRemoteManagement

Description

You will drive the success of clinical trials by leading complex statistical programming projects, ensuring high-quality data delivery while collaborating with cross-functional teams.

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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 specifications
  • •Advanced knowledge of CDISC data structures and standard programs
  • •Understanding of regulatory requirements like GCP or study procedures
  • •Communication, negotiation, and global influence skills
  • •Experience as Trial/Lead/Project Programmer and team coordination
  • •Initiative and cross-functional teamwork skills

Education

Bachelor's degree

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

Tools & Technologies

SASMACROsCDISC

Languages

English – Business Fluent

Benefits

Other Benefits

  • •Reasonable recruitment accommodations
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