Gupta - SAS,Base SAS, SAS Macro,SAS/SQL,MS Office,Excel,Power Point,Excel VBA,Medrio - Khanpur Extension, Sangam Vihar, New Delhi, Delhi, India

Mantu Gupta

Khanpur Extension, Sangam Vihar, New Delhi, Delhi, India

Summary

2 Year experience particularly in Clinical Research Organization (CRO) or Healthcare industry, knowledge of SAS, Base SAS,Macro, SAS/SQL. For Production and QC programming work in Clinical Trial Projects.Program derived datasets, tables, listings, graphs/figures (TLG), mostly in SAS, following the statisticial plan. Write validation programs electronically production versions of derived datasets and TLGs. Interact with Data management (DM) group to resolve data issues, including coding of adverse events and medications, etc. Work with Data Management (DM) group to make sure that any imported data from outside vendors or the client is an appropriate format and there is sufficient documentation available from the vendor. Document (track and update) all aspects of statisticial programming required for a clinical study for derived datasets and TLG generations. Interact with statisticians and other statisticial programmers in the team.
Analyse data with SAS and manipulate multiple datasets, aggregating data and merging datasets.
• Use import and export procedures to transfer data into different formats using SAS functions and arrays for manipulati
Maintain proper validation documentation to minimize redundancy in validation process.
• Generate report (tables, listings, and graphs) using PROC Report, PROC Tabulate, PROC Print & PROC Summary.
• Create custom reports generation using ODS (HTML, CSV, PDF and RTF).
• Definite best practices for project support and documentation.

Services

SAS,Base SAS, SAS Macro,SAS/SQL,MS Office,Excel,Power Point,Excel VBA,Medrio

Summary:

Job Description
• Maintain large data sets; combine data from various sources in varying formats to create SAS data sets files by using Set and Merge for generating Reports and Graphs.
• Extract data from database using SAS SQL procedure.

Work History

SAS Programmer

Vivante Technologies

From November 2012

As a leading hospital with pharmacology division involving in clinical research prime focus was on managing clinical data for analytical purpose. The analysis was based on the observations from real world CRF's. Reports include baseline history, status, analysis, follow-up visit, and drug safety reports as per protocols.
• Perform additional/ ad-hoc SAS programming support and produce analysis reports, tables, listings and graphs using both Large Pharmaceutical home grown system and custom SAS programs.
• Maintain proper validation documentation to minimize redundancy in validation process.
• Generate report (tables, listings, and graphs) using PROC Report, PROC Tabulate, PROC Print & PROC Summary.
• Create custom reports generation using ODS (HTML, CSV, PDF and RTF).
• Definite best practices for project support and documentation.
• Experience in information management technologies. Extensive hands-on experience and proficient knowledge in Designing & Developing flexible and scalable solutions using technologies like SAS/BASE, SAS/MACROS, SAS/ACCESS, SAS/CONNECT, SAS/GRAPH

Projects

Ad-Hoc Report

Responsibilities:
• Extracting data sets by using libname statement.
• Modified existing datasets using Set, Merge, Sort, Transpose and Update, Formats, Functions, Options and conditional statements.
• Involved in analyzing the raw data and planned for the programming logic to be created for the desired output.
• Cleaning, manipulating, Validation of data using Data step and Base SAS procedures.
• Perform additional/ ad-hoc SAS programming support and produce analysis reports, tables, listings and graphs using both Large Pharmaceutical home grown system and custom SAS programs.
• Develop SAS programs to create and validate statistical analysis datasets, listings and summary tables of safety and efficacy data, data extracts/ testing.
• Developed standard report for safety data including laboratory and adverse event summaries for IND (Investigational New Drug) updates using Proc REPORT and DATA _NULL_ steps.
• Developed routine SAS macros to create tables and listings for inclusion in Clinical study reports and regulatory submissions and to maintain existing ones.
• Accessing data from excel data base and SAS data sets\Importing the initial data set from the source file.
• Designing, building and testing in a series of SAS programs for generation of different data sets
• Generation of reports as per protocols.
• Developing reports using PROC REPORT, PROC TABULATE, PROC SQL, PROC FREQ and PROC MEANS.
• Generating graphs, gcharts for adverse events for each composition.

Qualifications & Certifications

Clinical Research Clinical Data Management & SAS

Cliniminds

MSc

Sikkim Manipal University

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