sas programmer

OBJECTIVE

Seeking a Data Management or SAS programmer/Data analyst position in public health and/or clinical trial field where extensive experience will be further developed and utilized.

CERTIFICATIONS

SAS Professional Certified Base Programmer for SAS V9 (April 2010)

SAS Professional Certified Advanced Programmer for SAS V9 (August 2010)

SUMMARY OF QUALIFICATIONS

•Proficient with Base SAS, SAS Macro and Proc SQL languages.

•Familiar with SAS reporting tools (proc print, proc freq, proc means, proc

tabulate, proc report, etc.)

•Experience using the SAS Output Delivery System.

•Program and validate clinical data set as specified.

•Knowledge of Excel, PowerPoint.

•Creative and positive team player with polished communication skills/writing skills.

•Resourceful in the completion of projects, effective at multi-tasking.

•Having many years working experience in clinical trials study.

PROFESSIONAL EXPERIENCE

Nutech Computer Training Institute, Inc. Rockville Maryland

Jan.2010- Feb.2011 Studying Base SAS Programming and SAS Macro, SQL Advanced Programming

•Inputted raw data into SAS using SAS data steps and SAS procedures.

•Used SAS Data Steps, Procedures Steps such as Proc Sort, SAS Macro, Proc SQL and SAS functions to cleanse, manipulate and combine datasets.

•Used SAS Output Deliver System (ODS) to present the reports in PDF, Excel and HTML formats

•Performed statistical analysis on data set and generated reports.

Finished Project and ongoing project:

•Tested how each of three different learning styles affects the academic achievement in ten high School students involved.

•Use SAS macro and sql technique to read seven years of birth-death files (csv data) in the District of Columbia to SAS data, then append and merge data sets. Examines the effects of neighbourhood disadvantage, individual characteristics such as race/ethnicity, age, low birth weight and behaviours (smoke and drinking) on infant mortality.

Aeras Global TB Vaccine Foundation

Research Associate Rockville Maryland

July 2010-Present

•Help Statistic Data Management Department to import clinic trial data (CSV data) to SAS data set.

•Validate the SAS data by using the Proc Compare SAS procedure and mainly using ODS RTF for generation of RTF output files.

•According to the STDM Specification to cleanse, manipulate and combine three data sets (ELISpot, Multiplex and FASCIA Data) into one SDTM.ZE.

•Validate the SDTM.ZE data and generate the ODS (RTF file) report to the

manager.

•Organizes, performs, and documents pre-clinical and clinical assays for vaccine studies. Implements and performs newly developed assays, including preliminary data analysis.

•Assists in assay qualification, validation, QA/QC procedures, and maintenance and updating of SOPs.

National Institute of Allergy and Infectious Diseases (NIAID) Vaccine Immune T-cell and Antibody Laboratory (NVITAL, contractor through HJF and LMC)

Gaithersburg, Maryland

Research Analyst Jan. 2008 – May 2010

•Performed immunoassays such as ICS, ELISA, ELSpot, HIV

Neutralization assays for the HIV Clinic trial samples.

•Report all results accurately and expeditiously, in compliance with SOPs and regulatory agency (cGCLP) guidelines.

•Perform preliminary data analysis and interpretation and verify correct data entry or further statistic analysis.

•Developed, wrote and reviewed SOPs.

SeraCare Life Science Inc and Medical college of Wisconsin

Research Associate Sep.1994 – Dec. 2007

•Performed various Immunoassays and EBV transformation and HPV transfection. QC Lyme disease detection kit (FDA approved) by using Western Blot method.

•Conducted site-directed mutants in FepA gene, which were included PCR, DNA sequencing and protein expression and purification.

EDUCATION

Bachelor of Science: Microbiology, Xiamen University Xiamen, China

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