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Saritha Pogadadanda

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68 views2 pages

Saritha Pogadadanda

Uploaded by

nandamahamkali
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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SARITHA POGADADANDA (MAIDEN NAME:BADARLA)

[email protected]
919.749.5695

SUMMARY:

 SAS Certified Base and SAS Certified Clinical Trials Programmer with 8+ years of experience in
Pharmaceutical and Clinical Research.
 Experience in SAS/BASE, SAS/MACROS, SAS/STAT, SAS/GRAPH, SAS/ACCESS and SAS/SQL
in Windows and UNIX Environment.
 Experienced in mapping CRF variables to SDTM and SDTM to ADaM variables.
 Wrote SAS programs for SDTM and ADaM datasets and Tables, Listings & Graphs (TLG).
 Developed and validated programs for derived analysis datasets and generated safety and efficacy
reports, listings and figures as per specifications in the Statistical Analysis Plan.
 Legal Status: US Citizen

EMPLOYMENT HISTORY

Jan 2019 – Present Senior Statistical Programmer


Covance Clinical Development Services, USA
 Ensures excellence in the delivery of analysis ready datasets, tables, listings, and figures to advance
research, development and following client SOPs and processes
 Optimized performance using Data Validation and Data Cleaning on Clinical Trials data using Statistical
procedures like PROC FREQ, PROC MEANS, and PROC UNIVERIATE Endpoints parameters such as
AUC, CMAX, TMAX for insulin and glucose using PK and PD profiles data
 Conducted various statistical analyses, by PROC GPLOT, PROC MIXED and PROC ANOVA
 Using SAS/ODS facility to create customized reports in HTML, PDF, RTF
 Extensively used SQL programming for joining multiple tables, sorting data, SQL views and indices
 Worked with statisticians, programming resources, and other colleagues as appropriate to ensure clear
specifications for programmed deliverables are in place
 Manage validation process and ensure good programming practices for quality of the statistical
deliverables
 Raise, discuss and resolve concerns/issues with relevant internal personnel
 Work cooperatively with study team members including but not limited to the biostatistician, lead
statistical programmer

Therapeutic Experience:

 Cardio Metabolic: Obesity Type II Diabetes (Phase I, II, III)


 Recently started working on Oncology studies.

May 2016 – Dec 2018 Sr. Statistical Programmer


Chiltern (Covance acquired), USA
 As Senior Statistical Programmer created, documented, and validated corresponding related SAS
programs, datasets, and outputs needed for the analysis which in a LSAF environment
 Produced safety and efficacy reports - tables, graphs, listing.
 Performed data manipulation techniques and advanced techniques (arrays,
Transpositions, complex merges, SQL, etc.) and generic macro use and
development to enable listing, table and graph generation
 Analyzed information and developed innovative solutions to programming and data analysis challenges
 Sound knowledge on generating report using Open CDISC validator Pinnacle 21 in addressing the issues.
 Efficiently produced quality results under time constraints
 Ensured the efficiency, quality, and integrity of data reporting and project activities executed
 Actively adapted and adjusted priorities to ensure timely and quality completion of
assigned tasks
 Performed other related duties as required by the Department
SARITHA POGADADANDA

Therapeutic Experience:

 Endocrinology: Phase II and III. Indication was Diabetes.


 Rare Genetic Disorder: Indication was the treatment of patients with a diagnosis of lysosomal acid lipase
deficiency – Registry Study

April 2014 – May 2016 Sr. Statistical Programmer


Cato Research
 Annotated Case Report Form (CRF) to SDTM standards Version 1.1 and 1.2
 Created Analysis Data sets from raw data using specifications developed from SAP.
 Created reports in RTF, PDF, Excel and HTML formats using ODS statements.
 Validated the datasets and compared the results to that of source programmer’s output.
 Interacted with statisticians, data managers to resolve data issues in conversion of SAS datasets into
SDTM-and ADaM-compliant structures.
 Produced Ad hoc reports of various kinds like Listings, Tables, and Figures (TLGs/TLFs) using Proc
Report, Proc Tabulate, Data _Null_ technique, Proc Gplot etc.

Therapeutic Experience:

 Endocrinology: Phase II, Multi site, Indication was Diabetes.

October 2011 – March 2014 Statistical SAS Programmer


Cato Research
 Mapped clinical trial data according to SDTM standards provided by the CDISC standards and expert in
understanding SDTM clinical domains.
 Used Open CDISC validator to check clinical data compliance with CDISC standards.
 Used SAS Macros extensively in the creation of new programs as well as modification of existing programs
to improve ease and consistency of results.
 Created TFL’s using SAS Procedures: REPORT, SUMMARY, TRANSPOSE, UNIVARIATE and MEANS.
 Validate programs and associated results produced by other programming colleagues using PROC
COMPARE, PROC CONTENTS and PROC FREQ. Frequently used SAS Options like DROP, KEEP,
RENAME, COMPRESS=, OBS= etc. for efficient programming and storage space saving when needed.

Therapeutic Experience:

 Cardiovascular: Phase III, Indication was Primary Hypercholesterolemia/Mixed Dyslipidemia.

EDUCATION

 Master of Science degree, Bioinformatics, GEORGE MASON UNIVERSITY, Old Town Manassas,
Virginia/VA/USA
 Bachelor of Science, Biology, NAGARJUNA UNIVERISTY, Vijayawada, Andhra Pradesh/AP/INDIA
 SAS Certified Clinical Trials Programmer Using SAS 9
 SAS Certified Base Programmer for SAS 9

ADDITIONAL SKILLS

 Databases: PL/SQL, Oracle, SQL Server 2000 and MS Access.

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