• Serve as Statistical Programming Lead on assigned projects. • Lead programming teams to deliver high‑quality outputs within agreed timelines and budget. • Drive project planning activities including start-up, resource allocation, and development of global programs and tracking tools. • Review statistical analysis plans (SAPs), mock shells, and database specifications. • Partner closely with sponsors, Biostatistics Leads, Data Management, and other stakeholders. • Monitor scope, resources, productivity, and project financials. • Support issue resolution and ensure smooth day‑to‑day study execution. • Develop and QC SDTM, ADaM datasets, analysis outputs, tables, listings, and figures. • Create and QC dataset specifications, study-level documentation, and regulatory submission materials. • Ensure all programming activities meet corporate quality standards, SOPs, ICH‑GCP, and regulatory requirements. • Demonstrate consistent first-time quality in deliverables through rigorous QC practices. • Maintain and deepen knowledge of global clinical and regulatory standards. • Mentor team members and provide project-specific training. • Lead knowledge-sharing initiatives across the department. • Maintain study documentation to ensure traceability and regulatory readiness. • Participate in audits and inspections as needed. • Contribute to process improvement, technology assessments, and operational optimization. • Provide expert programming consultancy to sponsors. • Represent Statistical Programming on cross-functional initiatives and external meetings.