Job Description
Job Title: Senior Statistical Programmer
Location: IN/EU(Hybrid/Remote)
Employment Type: Full-Time
Experience Required: 7+ Years
Job Summary
We are looking for a strong Senior Statistical Programmer. The role requires hands-on expertise in SAS-based analysis and reporting, CDISC-compliant SDTM and ADa M development, and delivery of high-quality Tables, Listings, and Figures (TLFs) in a regulated clinical research environment.
Key Responsibilities
Perform end-to-end statistical programming for clinical trial data analysis and reporting using SAS.
Lead the development, validation, and maintenance of SDTM and ADa M datasets in compliance with CDISC standards.
Program and validate Tables, Listings, and Figures (TLFs) for clinical study reports and regulatory submissions.
Support safety and efficacy analyses, including ISS and ISE deliverables.
Develop complex ad-hoc analyses and reports from raw clinical data.
Ensure production-quality prog...
Location: IN/EU(Hybrid/Remote)
Employment Type: Full-Time
Experience Required: 7+ Years
Job Summary
We are looking for a strong Senior Statistical Programmer. The role requires hands-on expertise in SAS-based analysis and reporting, CDISC-compliant SDTM and ADa M development, and delivery of high-quality Tables, Listings, and Figures (TLFs) in a regulated clinical research environment.
Key Responsibilities
Perform end-to-end statistical programming for clinical trial data analysis and reporting using SAS.
Lead the development, validation, and maintenance of SDTM and ADa M datasets in compliance with CDISC standards.
Program and validate Tables, Listings, and Figures (TLFs) for clinical study reports and regulatory submissions.
Support safety and efficacy analyses, including ISS and ISE deliverables.
Develop complex ad-hoc analyses and reports from raw clinical data.
Ensure production-quality prog...
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