OBJECTIVE: Seeking Senior SAS programmer position in pharmaceutical/CRO/healthcare industries

Certifications: SAS Certified Base Programmer for SAS 9 in SAS Institute

SAS Certified Advanced Programmer for SAS 9 in SAS Institute

Professional Experience

Confidential

Top Pharmaceutical Company 01/2009 Now

Biostatistician/Senior SAS Consultant

• Review SAP, Annotated CRF, Protocol Clinical Study Reports CSR for individual studies and ISS/ISE Integrated Summary of Safety/Efficacy for pooled studies
• Created SAS datasets from databases by SQL Pass Through Facility Performed Data Edit/Check as needed to understand the structure and content of data, to ensure integrity and correctness of data displays
• Developing reusable or customized SAS macros for Data Cleaning, Validation, Analysis and Report generation, testing and debugging existing macros
• Participates in the maintenance development of SOP standard operating procedures
• Programmed customized data displays including data listings, summary tables and routine graphics in accordance with approved SAP and table shells for clinical research studies
• Created mapping specifications from CRF data to SDTM, Generated SDTM data according to the above mapping spec and SDTM Implementation Guide v3.1.1
• Create Data specifications for Safety Analysis
• Review data Specifications for the Efficacy Analysis
• Create or validate the Derived Datasets for the Safety Analysis such as Demographics ADSL , Adverse Events ADAE , Electronic cardiograph ADEG etc and efficacy analysis such as ADSF, ADEF etc
• Performing safety analysis, efficacy analysis for both primary and secondary endpoints based on SAP Statistical Analysis Plan , CRF Case Report Form and Protocols
• Generating descriptive statistics using PROC MEANS/FREQ, and creating quality customized reports including TLF Table/Listing/Figures with PROC REPORT / TABULATE / SUMMARY
• Prepare the e-submission such as SAS Transport Datasets xpt and define.pdf
• Attended Biweekly meeting with Biostatisticians and SAS Programmers

confidential

Senior SAS Programmer

• Edited/Checked the quality of the clinical raw data
• Developed SAS macros for data cleaning Editing/Check
• Developed and reviewed SDTM Data Mapping Specification according to study CRF, protocol, annotated CRF, and SDTM Implementation Guide/Standard
• Developed SAS programs to map raw data into SDTM dataset according to SDTM Mapping Specifications
• Created reviewed Part of Data Specifications for Efficacy Analysis Safety Data Analysis
• Created derived data sets for the safety analysis such as Demographics ADSL , Adverse Events ADAE etc.
• Created part of the Derived Data Sets for the efficacy analysis
• Created Ad-Hoc reports using Proc Freq, Proc Print, Proc Means etc
• Created Table/Listing/Figures TLF for both the safety and efficacy analysis
• Cross-validated derived data sets / programs / outputs from other SAS programmers
• Created the summary and tables using Proc Report, DATA Null or ODS output
• Created Graphs by Proc GPLOT and Data Annotations
• Attended Weekly meeting with Biostatisticians.
• Analyzed clinical data and generated graphs using PROC LIFETEST, PROC PHREG, and customized MACROs
• Prepared/updated outputs for CSR Clinical Study Report

confidential

Senior SAS Programmer

Created SAS datasets from databases by SQL Pass Through Performed Data Edit/Check as needed to understand the structure and content of data, to ensure integrity and correctness of data displays Worked closely with statisticians and other programmers to develop comprehensive statistical analysis plans SAP Programmed customized data displays including data listings, summary tables and routine graphics in accordance with approved SAP and table shells for clinical research studies Quality controlled QC the output generated by other programmers Reviewed and commented Data Specifications for Safety Analysis Handled miscellaneous tasks assigned by management team Prepared documentations for programs Prepared documentation describing all datasets and variables within, including derived variables, and the project as a whole Created project specific macros and formats Liaised with external contract vendors Prepared data to be sent to CRO for Analysis Participated in the development, implementation and improvement of SOPs

confidential

Senior SAS Programmer

• Imported data from Excel files, Access Databases, text files, and other databases into SAS by PROC IMPORT / INFILE / CARDS / INPUT or SQL PASS-THROUGH
• Use SAS application developments for some easy-going data ETL Extracting / Transforming / Loading
• Created clean and validate data by Edit Check CRF
• Generate the Derived Data Sets according to SAP and Data Specifications
• Generated Table, Listing Figures according to TLF shells
• Pulled out data from clinical database prepare customized analysis datasets for specific reporting needs
• Generated Ad-Hoc reports including tables, listings and graphs outputs in HTML, RTF, PDF files for meetings and progress reports
• Performed ISS/ISE analysis, produced safety tables, listings and figures including summaries of DM, CM, MH and AE/TEAE etc
• Prepared for e-submission such as Transport files, define documents, formatted HTML and PDF reports using SAS ODS output delivery system

COMMUNICATION

• Strong verbal, written, and interpersonal communication skills
• Willing to collaborate with a cross-functional teams, drive and implementation and execution of projects
• Work well with technical supervisors and project managers
• Work independently and efficiently as well as a team player
• High level of writing and presentation skills