Associate Analyst, Statistical Programming

Responsibilities Support coordination, delivery, and review of statistical programming outputs across assigned studies Develop CDISC ADaM analysis datasets and specifications; identify and flag data quality issues Contribute to end-to-end programming from CRF data collection through regulatory submission Support preparation of submission deliverables (define.xml, XPTs, reviewer documentation) Collaborate with Biostatistics, Data Management, and Data Standards to ensure consistency and compliance Assist with process improvement initiatives and departmental efficiency efforts Requirements Bachelor’s degree in Statistics, Mathematics, or related field 0–2 years of SAS programming experience (Base, STAT, GRAPH, MACRO) Exposure to clinical trials, data management, or statistical analysis Basic knowledge of CDISC standards and clinical data structures Understanding of drug development process and regulatory requirements #J-18808-Ljbffr