sas programmer

Phillip Gao

Tel: 610-***-****

Email: ******@*****.***

Objective: A challenge position as a Statistical Programmer

Professional Skills

• 6+ years experience SAS Clinical programming

• Analyzed Phases I, II and III of Clinical Trials.

• Experience in all aspects of programming in clinical trials: data analysis, summarization, reporting.

• Generated independent SAS code for validation of other programmers' code, following SOP guidelines.

• Excellent communication, analytical and problem solving skills.

• Capable multitasks.

Work Experience

Statistical Programmer August 2009—Dec. 2009

Novartis. East Hanover NJ

• Worked in Phases I – III for Clinical Trials. Worked with Statistician to create derived dataset, tables, listings, figures and patient profiles

• Integrated databases from multiple studies or sources.

• Generated independent SAS code for quality checking of other programmers' codes, follow RAP guidelines for checking of data and programming integrity.

• Created SAS programs and macros to generate Efficacy and Safety tables.

Statistical Programmer June 2006---June 2009

Outsourcing Group for GSK, Clinforce Inc. Philadelphia PA

• Work in Phases I – III for Clinical Trials. Worked with Statistician to analyze the clinical data, tables, listings, patient profiles to support clinical activity and generate reports and graphs and enhancing output with ODS to generate reports in RTF and PDF formats.

• Ad hoc analyses, presentations, and data checks as appropriate.

• Generated independent SAS code for quality checking of other programmers' codes, follow RAP guidelines for checking of data and programming integrity; reviewing log messages.

• Validated the outputs for tables, listings and reports.

Statistical Programmer June 2005--June 2006

Ventana Clinical Research Group, Toronto, ON, Canada

• Provided SAS Programming in Clinical Trials (Phases I – III).

• Performed databases cleaning and validation; Created analysis data sets, safety and efficacy reports including Tables, Listings and Figures based on protocols and SAP.

• Created ad-hoc reports for interim analysis and for special purpose such as sub-group analysis.

SAS Programmer /Data Analyst

May 2003—May 2005

Biovail Contract Research, Toronto Canada

• Produced listings and tables and figures from specification according to study protocols including (but not limited to) Bioequivalence and Bioavailability studies

• Maintained SAS datasets, accessed various databases to collect data, performed table lookup operations and translated data values for meaning and readability.

• Data transmission and integrity check of the SAS datasets

Education

BSc Degree, Major: Statistic York University Canada 2000---2003

BSc Degree, major: Electrical Engineering Tianjin University China 1986---1990

Contact this candidate