Karthik Gadi is a clinical SAS programmer with over 3 years of experience developing applications in SAS. He has good knowledge and understanding of CDISC standards like SDTM and ADaMs. He has experience performing CDISC mappings, validating datasets using Pinnacle 21, and converting SDTM datasets to .xpt format. He is proficient in SAS procedures like PROC SORT, PROC MEANS, PROC FREQ and can produce customized reports using PROC REPORT. He has worked on multiple clinical projects involving tasks like data mapping, table development, and report generation according to FDA regulations.

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Karthik Gadi
(SAS Programmer)
Mobile:09704288856 Email:karthikgadi54@gmail.com
.
Professional Summary
 Having 3.7 years of experience in developing applications in SAS window
environment
 Good understanding of CDISC Standards for SDTM & ADaMs.
 Good knowledge of CDISC standards like SDTM(3.2) Domains and ADaMs (2.1)
 Data Transfer Specification (Spec writing), eCRF annotation.
 Performed CDISC SDTM Domain mapping for SDTM classification such as Special
purpose, Event, Intervention, Findings and Findings about.
 Performed CDISC ADaMs Domain mapping for ADaMs classification such as
ADSL, BDS and Non BDS.
 Good Understanding knowledge in Pinnacle 21 (Open CDISC Validation) tool For
Validating SDTM and ADaMs CDISC Standards.
 Having Knowledge in Efficacy, Safety and Summary Tables.
 Converting the SDTM datasets into .xpt formats.
 Experienced in producing PDF, RTF and HTML formatted files using SAS ODS
facility.
 Have good knowledge on SAS/BASE, SAS/MACRO, SAS/SQL, SAS/ODS.
 Worked with SAS Procedures such as PROC SORT, PROC MEANS, PROC FREQ PROC
TRANSPOSE, PROC PRINT, PROC REPORT etc.
 Produced quality customized reports by using PROC REPORT and also provided
descriptive statistics using PROC MEANS and PROC FREQ.
 Understanding on Analysis procedures (PROC CORR, PROC REG, PROC SGPLOT).
 Good Knowledge on protocol.
 Good Knowledge on FDA/ICH Guidelines.
 Combining and modifying existing datasets using merge, update and conditional
statements.
 Ability to understand the business requirements, client interaction and to do the
required analysis.
 Extensive experience in handling multiple projects in given timelines and budgets.

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Education
 M.Pharmacy (Pharmacology)SRI VENKATESWARA UNIVERSITY IN THE YEAR 2011.
Career Profile
 Worked as a clinical SAS Programmer(Research Assistant) for SUVEN LIFE
SCIENCES pvt ltd FROM AUG-2012 TO NOV-2014.
 Working as a clinical CDP Programmer for Quintiles India Research Pvt Ltd.
FROM AUG-2015 TO Till Date.
Technical Expertise
 Efficiency in the following modules of SAS system:
o SAS/BASE
o SAS/MACRO
o SAS/ SQL
RESPONSIBILTIES:
 Creating CDISC mapping for current trials and classified data into domains such AS
Demographics (DM), Disposition (DS), Medical History (MH), Adverse Event
(AE),Concomitant Medication(CM)
 Modified existing datasets using Set, Merge, and Sort, update, Formats,
Functions, Conditional statements and procedures.
 Experience in data mapping from non-CDISC SDTM to SDTM and From SDTM to
ADAM Standards.
 Programming analysis datasets in ADAM model, created tables by using ADAM
datasets.
 Involved in the development of tables – Demographic data tables, Subject
Disposition, Adverse Events tables, Medical history tables etc.
 Involved in multiple projects and interacted with other Programmers,
statisticians and data managers to analyze data.
 Created reports using the PROC REPORT for the submission as per the FDA
regulations and company standards.
 Formatted RTF reports using SAS/ODS (Output Delivery System).

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Strengths
 Excellent teamwork, analytical and problem solving skills.
 Ability to work independently under minimal guidance.
 Excellent communication skills.
DECLARATION
I hereby declare that all the information given above is true to the best of my
knowledge.
(KARTHIK.G)