Clinical Statistical Programmer
Preferred Educational Qualification for the role: Bachelor’s or Master’s degree or equivalent in statistics, mathematics, life science, engineering, or computer related subject.
Preferred experience for the role:
Professional with minimum 3 years of relevant experience in Statistical/SAS Programming in clinical domain.
Experience and understanding of ICH GCP principles and clinical drug development process.
Sound knowledge of CDISC SDTM and ADaM standards.
Good experience in multiple therapeutic areas and across multiple phases of clinical trials.
Experience managing integrated data analysis (ISS/ISE) is an asset.
Skills required :
Computer Literate (good knowledge of MS Office).
Analytical thinking ability.
Good problem solving and decision-making skills.
Time management skill.
Advance knowledge of Base SAS, SAS/STAT, SAS/Graph modules and SAS Macros.
Good communication and presentation skill.
Create and/ or review derive data specifications as per the standards for SDTM, ADaM datasets and pooled analysis (ISS/ISE) datasets.
Perform development and validation of analysis dataset, tables, listings, and figures for both safety and efficacy parameters.
Understand and comply with ICH-GCP guidelines, core operating proced
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