1. 1
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.

2. 2
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).

3. 3
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)