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XXXXX Mob No: +91-: Cytogenomics India Pvt. LTD

This document contains a summary of an individual's experience working as a SAS programmer for Cytogenomics India Pvt. Ltd since 2011. Key skills and responsibilities include clinical data management and analysis using SAS software, generating reports and tables from raw data as required by clients, and applying macros for reporting. Previous experience includes a 6 month project analyzing Phase I clinical trial data and generating required reports.

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272 views4 pages

XXXXX Mob No: +91-: Cytogenomics India Pvt. LTD

This document contains a summary of an individual's experience working as a SAS programmer for Cytogenomics India Pvt. Ltd since 2011. Key skills and responsibilities include clinical data management and analysis using SAS software, generating reports and tables from raw data as required by clients, and applying macros for reporting. Previous experience includes a 6 month project analyzing Phase I clinical trial data and generating required reports.

Uploaded by

rafielectronics
Copyright
© Attribution Non-Commercial (BY-NC)
We take content rights seriously. If you suspect this is your content, claim it here.
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XXXXX

Mob no: +91E-mail : @gmail.com

EXPERIENCE Working as SAS programmer in Cytogenomics India Pvt. Ltd, Bangalore from April 2011 to till date. SUMMARY Having 1.7+ Years of experience in analyzing, developing and implementing of various applications in SAS for Pharmaceutical. Strong proven knowledge in SAS/Base & Advance, SAS/MACRO, SAS/SQL, Excel. Extensive knowledge in data management like Merging, concatenating, interleaving and moving of SAS datasets. Strong working knowledge on BY group processing. Strong working knowledge on analysis of clinical trial data, generating reports, tables, and listings as per company standards. Experience on various procedures Proc datasets, Proc means, Proc sort, Proc freq, Proc Transpose etc. Generating reports as per clients specifications. Highly capable to learn quickly new technology and adapt to new environment.

Technical Skills: SAS Products : SAS/BASE, SAS/MACROS, SAS/SQL, SAS/STAT, SAS/ODS

[Data Extraction; Data Validation; Data Modification; Data Management; Data Analysis & Data Reporting using DATA & PROC Steps in SAS] Languages : SAS, SQL, Tools : MS Office Advanced EXCEL (Pivots, Charts, V-lookup, H-lookup, Functions & more); PowerPoint, Word, Outlook; Databases : Oracle, MS-Access Operating Systems : Windows 95/98/ XP SAS BI Tools : SAS/Enterprise Guide

EDUCATION MBA from JNT University-2010 B.Sc from SK University-2008

PROJECT PROFILE Project #2 Title Client Environment Platforms : Clinical Data Management (Dec 2011- till date)

: U.S Based : : Base SAS, SAS/Macros, SAS/SQL, Excel Windows

Description: This is a leading biopharmaceutical company in the field of pharmaceutical drugs, discovery and development. The Clinical statistical analysis involves assisting in the development of data analysis, planning and collaboration with statistical colleagues, physicians and other medical and paramedical staff. They are also responsible for working with system analyst to establish a reporting database and analyze the clinical trial data. The investigators collect the clinical data in CRFs (case report form or clinical report form) format. The data is sent to us as raw clinical data. This raw data, we study and create SAS datasets. Reports will be generated according to the FDA requirements and then macros are used to generate multiple reports. Responsibilities: Prepared new Datasets from raw data files using Import Techniques and modified existing datasets using Set, Merge, Sort, and Update, Functions and conditional statements. Cleaning, sorting and merging techniques is done using SAS/Base and SAS/Macros. Generating listings & reports by using the Proc report, Proc tabulate, Proc SQL. Generating Tables & reports by using the Proc Freq, Proc means, Proc Transpose, Proc SQL and Proc report. Application of Macros in summary tables.

. Project #1 Title Client Environment Platform Description: : : : : Analysis of Phase-I Data U.S Based

(Apr 2011-Dec2011)

Base SAS/Base & Advance, SAS/Macros, SAS/SQL, SAS/STAT Windows

This is a company developing products designed to improve the safety of the worlds health in Diabetes and is conducting Phase I clinical trials. The data is provided in the form of excel sheets. As a Statistical Programmer, my role was in analysis of clinical trials data and generating required reports, listings, summaries. Responsibilities: Developed SAS Programs based on wide usage of SAS/BASE, SAS/MACRO facility to generate tables, listings, reports for clinical studies. Involved in Delivering output using ODS (Output Delivery system). Using the Statistical procedures like Proc means, Proc freq, and Proc univariate and Proc Transpose. Personal Skills: Excellent written and communication skills Ability to analyze and interpret information Remarkable willingness to learn new aspects Strategic thinking with an analytic and creative mindset Strong interpersonal and leadership skills Ability to present complex information in a clear and concise manner Highly motivated, able to operate under high pressure and deadlines Ability to work effectively as a member of team and faster team spirit in others

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