Senior / Principal Statistical Programmer with Minimum (6 Months to 1 Year) of R programming.

nExperience

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- Senior Statistical Programmer: 7+ years
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- Principal Statistical Programmer: 9+ years
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nRole Summary

nResponsible for end-to-end statistical programming activities for clinical studies, from specification creation through regulatory submissions, ensuring high-quality and compliant deliverables.

nKey Responsibilities

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- Develop and validate SDTM, ADaM, and TLFs.
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- Create and review programming specifications.
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- Support regulatory submissions and ensure CDISC compliance.
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- Perform QC and maintain programming standards.
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- Collaborate with cross-functional teams and support study deliverables.
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- Contribute to process improvements and mentoring activities.
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nRequired Skills

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- Solid SAS programming expertise; Minimum 1 Year of R programming.
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- Hands-on experience with SDTM, ADaM, TLFs, and regulatory submissions.
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- Good understanding of CDISC standards and clinical trial processes.
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📌 Sr/Pr Statistical Programmer (7+ Years) with R(6 Months)
🏢 Trigent Software - Professional Services
📍 Gurugram