Job Description
About the Role
Looking for a Senior Statistical Programmer with strong hands-on expertise in SAS and R to support end-to-end clinical trial programming activities. The role involves working on SDTM, ADaM, TLFs, and regulatory submissions, collaborating closely with statisticians and clinical teams to deliver high-quality, submission-ready outputs.
Experience Requirements
- 6+ years of experience as a Statistical Programmer
- Strong hands-on SAS programming experience
- Minimum 2 years of hands-on R programming experience (mandatory)
- R-only knowledge or certifications without real project experience will not be considered
- Experience working with healthcare / pharmaceutical datasets
- Strong exposure to Clinical Research and Clinical Data Management
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