Anjali Kumari
DNO 15-12-13, RAM SHARMA STREET, HANUMANPET, VIJAYAWADA, PIN: 520124.
Ph.:
(M) +91 9546258642 E-mail: anjali65214@gmail.com
To explore the software industry and learn as much as I can, in the process would like to pursue a carrier in the industry and grow along with the organization I work for.
Summary
·
Extensive knowledge on SAS/BASE, SAS/STAT,
SAS/MACROS, SAS/SQL, SAS/ODS.
·
Extensive knowledge on REPORT generating
procedures like PROC FREQ, PROC MEANS, PROC UNIVARIATE, PROC TRANSPOSE, PROC
FORMAT, PROC REPORT etc.
·
Knowledge on Generating Tables, Listings as per company standards and in compliance
with 21 CFR Part 11, FDA and other regulatory compliance.
·
Knowledge ON CDISC SDTM.
·
Knowledge on analysing the data, generating
reports, tables, listings and graphs.
·
Knowledge on Phase-II & Phase-III Clinical
Trials, performed clinical data analysis and generated SAS datasets in
accordance with the SOPs and guidelines.
·
Exposure to clinical trial data such as
demographic data, Adverse Events(AE), CM data, Laboratory data (Lab data) and Vital Signs.
·
Knowledge in Generating Output files in RTF and
PDF using SAS/ODSs.
·
Ability to work on multiple tasks and strong
interpersonal, analytical and presentation skills.
·
Excellent in analytical, presentation,
communication and work independently as well as in a team.
·
Educational Background in Clinical and
pharmaceutical field with very good knowledge of Biostatistics.
SDTM
·
Knowledge about classifying general observation class,special purpose
domains etc.
·
Good
understanding of CDISC SDTM models
and in converting legacy data to CDISC SDTM (Study
Data Tabulation Model) Standards.
· Having knowledge in Creating SDTM datasets as per CDISC SDTM Standards (3.1.2).
·
Performed
CDISC mapping for current trials and classified data into domains such as Demographics (DM), Concomitant Medication(CM),Medical History (MH),
Adverse Events (AE) ,Vital Signs(VS) ,Laboratory Tests Results(LB)..
·
Basic
Knowledge in Understanding CDISC Domain Specifications
·
Knowledge
in validating CDISC SDTM Domains by
using cdisc validator.
·
Basic
knowledge in understanding of Study
Protocols, SAP (Statistical analysis plan), and CRF’s.
· Knowledge in Creating SDTM datasets for safety and efficacy domains
TECHNICAL
PROFICIENCIES:
SAS
Tools: V9.2, SAS /MACROS, SAS/SQL, SAS/STAT, SAS/ODS.
SAS
Procedures: Report, Print, Freq, Means,
Summary, Univariate, Sql, Sort, Transpose
Contents, Options, Import, Export,
Format, GPLOT.
Operating System: Windows,linux.
Office
tools:
MS-OFFICE,MS-ACCESS,MS-WORD,MS-EXCEL.
Strengths:
· Ability to deal with people diplomatically
· Highly motivated with a keen understanding of the
latest technologies and an inherent passion for Learning.
· Self-motivated and Self-managing. Results
oriented.
· Positive attitude and enthusiastic in teamwork.
· Ability
to handle crunch situations and adapt to any environment.
· Quick adaptation to new ideas and
methodology.
Academia:
· b. Pharmacy from Nirmala College of
Pharmacy affiliated to Acharya Nagarjuna University, Guntur in 2013 with 72%.
· IPE from Narayana Junior College, Vijayawada in 2009 with
88%.
· SSC from Sri Kakatiya high school, Vijayawada in 2007 with
83.2%.
Extra
curriculum activities:
·
A postal presentation given in IPA CONVENTION
2012 in manipal university. and also
participated in various institutions.
·
Attented national seminar conferences.
·
Have participated in various Cultural activities
and achieved awards.
·
Have participated in various Quiz competitions.
·
Participated in blood donations camps conducted
by Red cross society.
·
Participated in NSS Camps conducted by our
institution.
Key
intreast:
· To make carrier as a clinical sas programmer
Project
done in my institute:
Therapeutic area: cardiology
Description:
A Double-Blind, Randomized, Placebo-Controlled ,multicentral, paralel assignment Trial to Evaluating The Safety And Efficacy Of the study drug .
Responsibilities:
- Responsible for creating tables and listings as per the sap
- Analyzing the clinical trail data with the use of various sas
products
- Responsible for report validation .
- Extensive usages of procedures like
means,freq,contents,sort,transpose format,compare.
- Extensive use of function
for clear the cosmetic errors
- Creating macros and usage of standard macros to optimize the
code.
- Creating user define formats by using proc format
- Create the reports with the use o proc report and tabulate
- Exporting the analyzed data to client based on requirement with
use of ods statement
Personal Dossier:
Linguistic Proficiency : English & Telugu
Location Preference : Anywhere in INDIA
(Anjali kumari)
.JPG)
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