Sreekanth - SAS Programmer - Hyderabad, AP, India

Kanumetta Sreekanth

Hyderabad, AP, India

Services

SAS Programmer

Summary:

Certified SAS Base Programmer with 2 Years of experience looking for a change

Work History

"BYGOMIN SR 1G"

Project IV

December 2013 - April 2014

Project Title: A single dose, two period, crossover, open labeled, randomized, bioequivalence study of test product; "BYGOMIN SR 1G" (containing Metformin HCL 1000 mg) of Vance & Health Pharmaceuticals Pvt. Ltd with reference product; "Obimet SR 1000 mg"(containing Metformin HCL 1000 mg) of Abott India Pvt. Ltd in healthy, adult, male human subject under fasting condition in randomized crossover design.

Job title: SAS Programmer

Duration: July 2013 to Nov 2013
Project III:

SAS Programmer

SG Phyto Pharma Pvt Ltd

February 2013 - June 2013

Clinical SAS Programmer

Sanjeevani Life Sciences

From June 2012

Skills Summary
Programming Languages: SAS (v9.2).
Databases: Oracle
SAS Tools: SAS/BASE, SAS/MACROS, SAS/Graphs, SAS/Access.
Certificate course: MS Office, C-language, OOP using C++, Core Java.

Projects Handled

Project V:

Project Title: A single dose, two period, crossover, open labeled, randomized, bioequivalence study of test product; " PROVAN" (containing Propranolol 40mg) of Vance & Health Pharmaceuticals Pvt. Ltd with reference product; "Inderal 40 Tablet"(containing Propranolol 40 mg) of Abott Healthcare Pvt Ltd (AHPL) in healthy, adult, male human subject under fasting condition in randomized crossover design.

Job title:SAS Programmer

SAS Programmer

Management of Migraine

August 2012 - January 2013

Project Title: A Parallel two armed, randomized, open labeled, Phase III Clinical study comparing the Palsinuron and Mahavatvidhwans ras in the Management of Migraine
(Ref: CTRI/2012/06/002739).

Project I:

SAS Programmer

Solar Herbo Pvt Ltd

February 2012 - July 2012

Project Title: An Open Label, Phase III Clinical Trial To Assess the Therapeutic Efficacy & Safety Of Malbet Capsules in the treatment Of Malaria
(Ref: CTRI/2012/08/002913).
Responsibilities:
⇨ Involved in managing randomized phase III clinical trials data.
⇨ Developed new and modified existing SAS programs to load data from the external source and create study specific datasets, which are used as source datasets for report generating programs.
⇨ Modified existing datasets using Set, Merge, Sort, and Update, Formats, Functions and conditional statements.
⇨ Developed SAS Programs for Data Cleaning, Validation, Analysis and Report generation.
⇨ Created and validated Tables, Figures, and Listings according to the Statistical Analysis Plan (SAP)
⇨ Created SAS Macros and modified the existing ones relating to multiple studies.
⇨ Used SAS/ODS for generating different output formats as requested.
⇨ Extracted data from Oracle using SQL Pass through facility and generated ad-hoc reports.
⇨ Involved in generating Safety tables (ISS) as per the requirements of the Statistician and SAP.
⇨ Attended project team meetings, worked with Bio-Statisticians, Data Managers, and Clinical Research Managers as appropriate. Reviewed and provided feedback for Data Integrity Plans.

Environment: SASBASE, SAS/STAT, SAS/MACROS, SAS/GRAPH, SAS/ACCESS, SAS/SQL and Windows.

Qualifications & Certifications

Biotechnology

Andhra University Visakhapatnam

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