OBJECTIVE
To work in a organization that utilizes my strong analytical and programming skills adding value to the organization and myself.
summary
- Having 3+ years of Experience in the field of SAS programming using Base SAS, SAS Macros and SAS/SQL on Windows.
- Extensively working as a SAS programmer.
- Hands on experience in presentation of Tables, Listing using clinical data.
- Well versed knowledge on ODS.
- Expertise in using SAS procedures such as Tabulate, Report, Transpose, Sort, SQL, Means, Freq and ODS.
- Understanding the Annotated CRF, Protocal and SAP.
- Generating the Safety and Efficaly tables by using SAS programming.
- QC for Generated Tables.
- Able to work in fast read Environment and deadlines.
- Ability in analyzing Business Requirements.
- Excellent Team player with good communication and inter-personal skills.
EXPERIENCE
- Working as a SAS Programmar for GVK Bio,
- Worked as SAS Programmar with Sonata software Ltd,
EDUCATION
- Bachelor of Science from
SKILLS
- SAS Tools : SAS/Base, SAS/Access, SAS/Macros
- M.S.Office Suite : Word, Excel, Access
- Operating System : Windows family
- Languages : SAS, SQL.
PROJECTS:- PROJECT#1
Project Title : Analysis of Metastatic.
Client : Medarex Pharma ,USA
Period : May 2007 to till date
Description:
Clinical Trials are conducted to study the effect of new medicine in the treatment of cancer disease. This study was a double blind randomized, multi-dose studies conducted in two groups of patients i.e., One in patient’s with metastatic Cancer disease and one in patient’s with hormone refractory prostate cancer. The trial was initially conducted on a total of 46 chemotherapy patients with metastatic disease. Patients were followed until tumor progression and were evaluated based on objective tumor responses. The data indicated that the product was generally well tolerated. Across both studies, mild to moderate adverse events, including a rash or itching were experienced in small number of patients. Further signs of immunologic activity directed at tumors included tumor necrosis, inflammatory reactions at tumor sites and immune mediated rash.
Responsibilities:
- Converted the clinical trail data, subject records entered in the database files to SAS data sets using SAS/Access.
- Developed SAS programs using Base SAS for tabulation counts, sorting and merging data validations using PROC Means, PROC Tabulate .
- Involved in the process and IT infrastructures for Phase II and III Clinical Trials. Ensured quality of dataset at the protocol level while working to deliver competitive advantage and cost efficiency to the company as a whole. Achieved these tasks by serving as member in data management team.
- Converted oracle data tables into SAS data files using SAS/SQL and uploaded SAS data files into oracle tables.
- Create programs for presentation of graphs using SAS/GRAPH. The presentation of graphs include create a text slides, display several graphs at one time, combine graphs and text in one display and create automated presentations.
- Closely work with the statisticians and scientists to identify common factors across the projects.
- Created programs for generating reports of clinical studies which include risk and odds rations, and significant multivariate factors using SAS/STAT.
Environment: SAS/ Base, SAS/ Macro, SAS/Access, SAS/Connect, SAS/Graph, SAS/Stat, Excel, Word, Windows 2000 NT.
PROJECT#2
Project Title : Analysis of Drugs.
Client : Telik , CA
Period : March’06 to April’07
Description:
Responsible for creating data sets, listings and reports for clinical trials data. Involved in validations edit checks and extensively used the procedures like REPORT, SUMMARY, TABULATE, FREQ, TRANSPOSE, UNIVARIATE, SORT and MEANS. Worked on safety, efficacy tables and created analysis tables and reports.
Responsibilities:
· Used SAS/Base to perform sorting, merging of clinical data and generated reports.
· Developed SAS Macros for loading database tables.
· Provided programming support for the creation and maintenance of programs used in data management, data validation, and statistical report generation.
Environment: Windows2000, SAS/BASE, SAS/STAT, SAS/GRAPH, .
PROJECT#3
Project Title : Analysis of DrugSystem
Client : Celgene Pharmaceuticals,USA
Period : Dec’04 to Feb’06
Description :
Involved as a clinical trials SAS Programmer. Responsible for creating SAS data sets using the raw clinical data for various analyses of safety and efficacy reports/listings. Involved in phase I and phase II clinical study safety reports. Extensively used SAS/Base, SAS/Macros and SAS/Access .
Responsibilities:
· Extracted data from the CRF database, created SAS data sets and prepared data model.
· Drawing flowcharts indicating the input data sets, sorting and merging techniques and writing SAS code accordingly.
· Converted SAS listings and tables into PDF, RTF, HTML formats to meet specifications by using SAS ODS.
· Provided data in SAS transport files, and other appropriate deliverables and documentation for regulatory submissions.
· Moved data sets across platforms.
Environment: Windows 2000/NT, SAS/Base, SAS/SQL, SAS/STAT, SAS/GRAPH, SAS/Access, SQL.
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