P. Shilpa
mail: shilpap***@gmail
Pharmacy Graduate
Mobile. No: 91-784*******
CAREER OBJECTIVE:
To associate with an organization that gives me an opportunity to gain
further exposure
and experience, improve my knowledge with the latest trends and to be a
part of the team
that works dynamically towards the growth of the organization.
SUMMARY:
. Proficient in SAS PROGRAMMING 9.2 on windows
. Proficient in Base SAS, SAS SQL, SAS-MACRO Language.
. Good knowledge on Importing and Exporting files using PROC IMPORT AND
PROC EXPORT, Data transformations, Data Validation Techniques.
. Proficient in User defined formats, GCHART, GPLOT, PROC TABULATE, and
PROC REPORT Procedures.
. Creating Tables, views, Indexes and maintaining Tables using SAS-SQL.
. Proficient Knowledge on SAS Macro programs and Macro Parameters
. Good Knowledge in Creating Macro Variables in SQL and DATA STEP.
TECHNICAL SKILLS:
. Office Packages : MS Office 2003 and 2007 (Word, Excel.
PowerPoint)
. Programming : SQL, SAS 9.2, MACRO.
WORK EXPERIENCE:
IDDCR, Hyderabad August 2012
to till date
Intern - SAS Programmer
Responsibilities:
. Reading Excel worksheets, delimited raw data files to SAS
. Sub setting Observations and variables and Adding Permanent attributes
. Good knowledge on combining SAS Datasets, Data validations, Data
Cleaning and manipulating data.
. Good Programming knowledge on Data Transformations, data summarization
and Debugging.
. Having knowledge on statistical procedures like PROC MEANS,PROC FREQ,
PROC UNIVARIATE.
. Creating and modifying Tables and views by using PROC SQL.
. Having Knowledge on combining tables using Joins - PROC SQL.
. Creation of macro variables, defining and calling macro, macro
functions
. Having knowledge on creating macro variables in a DATASTEP and PROC
SQL.
PROJECT EXPERIENCE:
Project - 1
TITLE 1: CUBICIN ; Outcomes Registry and Experience (CORE) for the
Treatment of
Serious Gram-positive Infections
Phase: 4
Drug: CUBICIN (daptomycin for injection)
Sponsor: Cubist Pharmaceuticals, Inc.
Responsibilities:
1. Validating and conversion of Non - CDISC SDTM Dataset to CDISC SDTM
Dataset as
per SDTM IG 3.1.2
2. Analytical Dataset (VS, MH, AE etc.,) creation as per ADS Specification
3. Used proc cdisc as SDTM VALIDATING TOOL
4. Developed SAS programs to create SDTM datasets
TITLE 2: A Randomized, Double-blinded, Placebo-Controlled, Single-dose and
Pharmacokinetic study of ascending doses of XYZ-123,001 in healthy
volunteers
Phase: 1
Drug: XYZ-123,001
Sponsor: XYZ Pharmaceuticals
Responsibilities:
1. Validating and conversion of Non - CDISC SDTM Dataset to CDISC SDTM
Dataset as
per SDTM IG 3.1.2
2. Created SDTM Mapping Specification
3. Developed SAS programs to create SDTM datasets
EDUCATION:
> Bachelors in Pharmacy ANANTAPUR University, NARAYANA pharmacy college,
Nellore from Sep 2008 to Oct 2012with 74.11%
> Intermediate,AP from 2006-2008 with 89.00%
> S.S.C,AP in 2006 with 87.33%
INTERNATIONAL CREDENTIALS:
Certified Base Programmer for SAS.9 (March, 2013)
KNOWLEDGE IN:
> ICH-GCP Efficacy guidelines: E3, E6, E9.
> 21 CFR Part 11.
> CDISC-SDTM.
> Good Clinical Data Management Practices (GCDMP).
.
PERSONAL DETAILS
Fathers Name : P. Rajasekhara Reddy
Date of Birth : 05-09-1991
Gender : Female
Marital Status : Single
Languages known: English, Telugu, Hindi
DECLARATION:
I hereby declare that all the details furnished herewith are true to the
best of my knowledge.
Date:
Place: Hyderabad Shilpa.P