Job TitleEngage directly with cross-functional teams and contribute to high-visibility clinical initiativesWork on-site in a collaborative setting that encourages knowledge sharing and technical excellenceLead programming efforts supporting clinical studies and regulatory deliverablesDevelop and validate SDTM and ADaM datasets in alignment with CDISC standardsProduce high-quality analysis outputs, including tables, listings, and figures for trials and publicationsCreate, maintain, and optimize SAS macros and utilities to enhance programming efficiencyDraft clear dataset specifications aligned with study protocols and analysis plansPartner with statisticians, data managers, and clinical teams to ensure accurate, timely outputsManage multiple complex assignments and drive them to completion with minimal oversightContribute technical expertise to problem-solving, workflow enhancements, and process improvementsGrow your experience in a setting that values innovation, problem-solving, and data accuracy8+ years of clinical or statistical programming experience within pharma, biotech, or related industriesAdvanced SAS programming skills with demonstrated expertise in dataset creation and validationDeep familiarity with CDISC SDTM and ADaM standardsPrior leadership experience supporting studies or overseeing programming deliverablesStrong understanding of clinical trial data structures and regulatory expectationsExcellent communication skills and ability to collaborate across cross-functional teamsBachelor's degree in Statistics, Computer Science, Mathematics, or a relevant scientific discipline