Sr/Pr Statistical Programmer (7+ Years) with R(6 Months)

Senior / Principal Statistical Programmer with Minimum (6 Months to 1 Year) of R programming.ExperienceSenior Statistical Programmer: 7+ yearsPrincipal Statistical Programmer: 9+ yearsRole SummaryResponsible for end-to-end statistical programming activities for clinical studies, from specification creation through regulatory submissions, ensuring high-quality and compliant deliverables.Key ResponsibilitiesDevelop and validate SDTM, ADaM, and TLFs.Create and review programming specifications.Support regulatory submissions and ensure CDISC compliance.Perform QC and maintain programming standards.Collaborate with cross-functional teams and support study deliverables.Contribute to process improvements and mentoring activities.Required SkillsStrong SAS programming expertise; Minimum 1 Year of R programming.Hands-on experience with SDTM, ADaM, TLFs, and regulatory submissions.Good understanding of CDISC standards and clinical trial processes. .