Sadhna S

About Sadhna S

Experience in Respiratory and Oncology TA.Leading Projects which includes coordinating with stakeholders, deciding on time lines, resource planning, reviewing metadata, guiding the team, Reviewing trial related documents (CRF, Protocol, Raw data) and SAP(statistical analysis plan) and any other study reporting activities,SAS/Statistical programming experience in all different phases of clinical trials in pharmaceutical.Experienced in various therapeutics areas.Proficient in SAS/BASE, SAS/MACRO, SAS/GRAPH, SAS/SQL, SAS/ODS, and SAS/STAT.Extensive experience of data manipulation techniques such as merging, concatenating, and interleaving of SAS datasets using both SAS DATA steps as well as PROC SQL.Developed and debugged SAS Macros for creating tables, graphs or datasets.Well experienced in program validation & quality check (QC) activities. Contributed in preparing various clinical trial reports, and professional presentations.Programmed/validated tables and/or graphs for Integrated Summary of Safety (ISS) and Integrated Summary of Efficacy (ISE).Formatted PDF, RTF, & HTML reports using SAS/ODS.Good working knowledge of clinical trials data in the domains of demographics, disposition, adverse events, laboratories, vital signs, and efficacy.CDISC-SDTM, ADaM data conversion and TLF\'s, Clinical SAS programmer, SAS Macros, Unix.Knowledge of Pinnacle and ADaM Reviewers Guide.Knowledge of CRT Packages. Knowledge of Define1.0 and Define 2.0 version.

Experience

1. Statistical Programming Associate Director

   AstraZeneca

   Jan 2025 — Present

Skills

• Validation
• Pharmaceutical Industry
• Advance Sas
• Base Sas Certified
• Cdisc
• Sas Sql
• Sdtm
• Adam
• Sas Base
• Sas Macro
• Microsoft Office
• Clinical Trials
• Clinical Research