Senior Statistical Programmer

• Contribute to or lead statistical programming activities for Phase I to IV clinical trials. • Develop and validate datasets, tables, listings, and figures (TFLs) according to specifications. • Build and maintain effective working relationships with cross-functional teams (e.g., biostatistics, data management, clinical teams). • Participate in team meetings and communicate programming progress and issues. • Adhere to company, departmental, and industry standards (e.g., CDISC SDTM/ADaM, GCP). • Ensure audit readiness and compliance with regulatory requirements. • Review or develop programming specifications as part of statistical analysis plans. • Participate in or lead the review of eCRFs and data structures. • Ensure accuracy, reliability, and quality of statistical analysis results.…