Zentalis Pharmaceuticals

• Preparing clinical and statistical reports using SAS; • Creating tables, listings, figures (TLFs) and analysis datasets to support medical and clinical review, and to enable the data-driven operation and decision in oncology-related clinical trials; • As the owner of business intelligence, communicating with management and project teams for report requirements and specifications and standardize the basic reports in supporting the Risk-based Monitoring and solving operational or data problems for clinical trials; • Working with study statisticians to support abstracts, posters, manuscripts and other oncology related clinical publications; • Understanding Clinical Data Interchange Standards Consortium (CDISC), Study Data Tabulation Model (SDTM) and Analysis Data Model (ADaM) standards and regulatory requirements; • Creating SDTM/ADaM datasets while following CDISC standards; • Developing independent programs to validate analysis datasets and TLFs generated by vendors, ensuring compliance with CDISC and submission requirements; • Working on oncology studies to perform safety and efficacy analysis; • Developing and maintaining SAS programming macros, templates and utilities to support internal data review, monitoring, data reporting and visualization.