Found Description
Elevate your career as a Lead Principal Statistical Programmer, focusing on high-quality programming solutions for clinical studies. Collaborate with SAS programmers and Biostatisticians in a dynamic environment.
In this critical role, you will leverage your expertise in SAS programming and leadership to oversee a team while delivering robust analytical solutions in various therapeutic areas. With a strong foundation in CDISC, SDTM, and ADaM standards for Phase 2-3 trials, your experience will directly impact clinical data analysis and project management.
Key Responsibilities:
• Act as the Lead Programmer overseeing project teams
• Author, review, and update SDTM specifications and datasets
• Collaborate on ADaM specifications and review TLFs
• Program detailed tables, listings, and figures for studies
• Conduct quality control checks to ensure data integrity
Requirements:
• BA or BSc in Statistics or Math
• Minimum 7 years of SAS experience in clinical pr...
In this critical role, you will leverage your expertise in SAS programming and leadership to oversee a team while delivering robust analytical solutions in various therapeutic areas. With a strong foundation in CDISC, SDTM, and ADaM standards for Phase 2-3 trials, your experience will directly impact clinical data analysis and project management.
Key Responsibilities:
• Act as the Lead Programmer overseeing project teams
• Author, review, and update SDTM specifications and datasets
• Collaborate on ADaM specifications and review TLFs
• Program detailed tables, listings, and figures for studies
• Conduct quality control checks to ensure data integrity
Requirements:
• BA or BSc in Statistics or Math
• Minimum 7 years of SAS experience in clinical pr...
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