Job Description
Senior / Principal Statistical Programmer with Minimum (6 Months to 1 Year) of R programming.
nExperience
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Senior Statistical Programmer: 7+ yearsn
Principal Statistical Programmer: 9+ yearsn
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.n
Create and review programming specifications.n
Support regulatory submissions and ensure CDISC compliance.n
Perform QC and maintain programming standards.n
Collaborate with cross-functional teams and support study deliverables.n
Contribute to process improvements and mentoring activities.n
nRequired Skills
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Robust SAS programming expertise; Minimum 1 Year of R programming.n
Hands-on experience with SDTM, ADaM, TLFs, and regulatory submissions.n
Positive understanding of CDISC standards and clinical trial processes.n