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Lead Statistical Programmer
1 week ago
Responsibilities:
- Providing statistical input to the design, analysis, reporting and interpretation of clinical studies and contribution to publications
- Plan and manage programming activities across multiple studies to deliver all data analysis outputs with quality
- Developing, maintaining and validating SAS programs/macros for study specific analyses or at the standard level.
- Writing specifications for SAS programs/macros for study specific analyses or at the standard level
- Responsible for programming and QC across a study including submission activities adhering to relevant SOPs / policies.
- Review and provide inputs into various study plans like SAP, TFL, CRF etc...
- Oversee outsourced activities to third party vendors to meet the agreed timelines, quality and budget requirements established for the project
- Develop specifications and SAS programs for the creation of SDTM and ADaM data sets as well as the supporting documentation needed as required by CDISC standards
- Review and ensures adherence to CDISC standards at the study
Qualifications :
- Masters in Statistics/Mathematics/Computer Science
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