SAS programmer

LIXIAO (Lisa) SU

New Brunswick, NJ Email: ***********@*****.*** phone: 732-***-****

OBJECTIVE: SAS PROGRAMMER

Seeking an entry-level SAS programmer position in a pharmaceutical or clinical trial related company where a highly motivated SAS programmer can make significant contributions.

EDUCATION:

Master Degree of Biostatistics, RUTGERS UNIVERSITY, SCHOOL OF PUBLIC HEALTH, GPA: 3.9, 2014-2016

Master of Medicine, BEIJING INSTITUTE OF HEART LUNG AND BLOOD VESSEL DISEASES 2010-2013

Bachelor of Medicine, CHENGDE MEDICAL UNIVERSITY, 2005-2010

CERTIFICATIONS

SAS certificated Base programmer for SAS 9

SAS certificated Advanced programmer for SAS 9

Medical Certificate, 2011, China

PROFESSIONAL EXPERIENCE:

School of Public Health, Rutgers University, NJ May 2015 – Present

Statistical Research Assistant

Project of Observational study about Prostate Cancer. Clinical trial data from pharmaceutical company using SDTM Dataset.

Analysing the predictive relationship between pain and overall survival in patients with prostate cancer

Pooled data from 4 randomized, placebo-controlled trials.

Performing literature review and studying clinical trial protocols including CRF to design and conduct data analysis.

Cleaning and merging data for separate and joint survival and longitudinal analyses (PROC LIFETEST, PROC PHREG, PROC COX, PROC GENMOD, R)

Generated analysis data sets and developed SAS programs to generate analysis outputs as specified in the statistical analysis plan.

Writing SAS Macro and ODS procedures to create tables and perform tests to summarize and compare patient characteristic information (PROC TRANSPOSE, PROC MEANS, PROC FREQ, PROC UNIVARIATE normal, PROC TTEST, %MACRO.)

Graphing survival and longitudinal curves using R and SAS.

SUMMARY:

Master of Science in Biostatistics with strong statistic theory.

1 year statistician research assistant in Rutgers

Understanding the concepts and application of statistical methods used in design, conduct, monitoring, and analysis of clinical trials. Familiar with basic knowledge of FDA regulations.

Expertise in SAS (BASE, SQL, GRAPH, MACRO, ODS); R; SPSS; MS-DOS

Ability to analyse, model, and conduct statistical analyses

Ability to convert data from multiple, complex systems

Experience in creating table, listing, graph

Sample size calculation and randomization using R

Excellent written, oral, and interpersonal communication skills

Able to effectively manage multiple tasks and cooperate with team.

REFERENCES:

Shou-En Lu, Ph.D., Associate Professor of Biostatistics, School of Public Health, Rutgers University.

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