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Principal Statistical Programmer
Sandoz
posted 16d ago
Job Role Insights
Flexible timing
Key skills for the job
Job Description
- Determine an efficient project programming strategy that utilizes organization standards and procedures. Develop project-level programming specifications for analysis datasets and pooled datasets for a project.
- Lead the production of statistical outputs for clinical study reports, publications, and market promotions.
- Ensure the quality control of all programs, specifications, and statistical outputs within a study project.
- Ensure that programming-related documents are consistent, and comply with required standards, by reviewing case report forms, statistical analysis plans, data structures specifications, and specifications for tables, listings and figures. Archival of project programs and associated documentation. Mentor programmers in the functional expertise required for project support.
- Support the development of, and the training of users in, new programming applications.
- Proactively drive continuous improvements to departmental processes, standards and utilities. Support and Participate in Process initiatives/enhancements across Biometrics.
- Ensure that timelines are adhered and lead statistical programming team to successful completion of studies within given timelines .Develop advanced, general-purpose programming functions for deployment across multiple projects.
- Maintain advanced knowledge of programming languages (e.g., SAS and R).Manage the outsourcing of programming activities from Biometrics to an approved vendor in accordance with Scientific Services vendor management procedures.
- Graduation/Post graduation or equivalent experience in mathematics, statistics, computer science, or health sciences/related field.
- At least 8 years work experience in a programming role preferably supporting clinical trials/ or in the pharmaceutical industry (5 years for MS Statistics / Computer Science graduates with excellent understanding of CDISC SDTM and ADaM standards).
- Advanced knowledge of / experience with SAS and/R, and other relevant programming software.
- Proven experience in development of advanced programming functions with high programming efficiency; strong programming and problem-solving skills Proven experience in leading programmer support for multiple clinical trials and submission activities (or equivalent)
Desirable Requirements:
- Good understanding of global clinical trial / project practices, procedures, methodologies.
- Good understanding of regulatory requirements relevant to statistical programming (e.g. Good Clinical Practice).
Employment Type: Full Time, Permanent
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Sandoz Benefits
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