clinical sas programer

Sathish K

Phone: +91-630******* E-Mail:***************@*****.***

Seeking assignments in SAS Programming with a growth oriented organization of repute.

PROFESSIONAL SYNOPSIS

Having 2.0 years of Experience as a SAS Programmer.

Experience in working with SAS/BASE, SAS/MACRO, SAS/STAT, SAS/ ODS, SAS/ SQL

Thorough Knowledge in using SAS procedures such as : PROC MEANS, PROC FREQ, PROC REPORT, PROC SORT, PROC TRANSPOSE, PROC FORMAT, etc.,

Thorough knowledge in SAS Programming, merging SAS Data Sets, Preparing ADS, Producing Reports.

Clinical data knowledge including exposure to CDISC (SDTM, ADaM), analysis data specification, analysis data set creation, Safety outputs.

Profound experience in working on Demographics, Adverse events, Disposition, Conmed and Medical history data.

Good understanding of the procedures in Phases I, II, and III clinical trials studies in various therapeutic areas.

Highly energetic, creative, self-motivated with proven interpersonal, negotiation, communication skills and Strong presentation and leadership skills.

Dedicated and highly ambitious to achieve personal goals as well as the organizational goals.

Participated in project meetings and team player with problem solving and analytical skills.

WORK EXPERIENCE

Working as Associate executive Statistical Programmer from feb-2018 to till now in ClinDataCeutics Pvt Ltd, Hyderabad.

MY STRENGTHS

Passion for work is my greatest asset besides excellent communication skills and interpersonal skills.

EDUCATIONAL QUALIFICATION

Graduation in civil Engineering from Jawaharlal Nehru Technological University (JNTU), Hyderabad.

IT SKILLS

Operating Systems : Windows 95/98/2000server

Languages : SAS, SQL

RDBMS : MS Access

Software Applications : SAS and MS Office.

SAS EXPOSURE

SAS SKILLS : SAS/BASE, SAS/SQL, SAS/MACROS, SAS/STAT.

PROJECTS HANDLED

PROJECT II

Therapeutic area: ONCOLOGY

ROLE: SAS Programmer.

Responsibilities:

•Good Knowledge on Creation of SDTM data sets based on SDTM 3.1.2 and SDTM 3.2

•Creation of AdaM Datasets based on the given specification document, SAP and mock shells.

•Generating Safety Tables and Listings based on the given mock shells.

•validating the Data sets,Tables and listings using Double programming.

•Creating the user level macros and using the standard macros and study level macros.

•Involving Study level meetings and raise the issues to related team.

•Attending the knowledge sharing sessions with in the team and other teams.

PROJECT I

Therapeutic area: ONCOLOGY

ROLE: SAS Programmer.

Responsibilities:

Experience in CDISC SDTM mapping of variables to make the raw data confirmed to SDTM model.

Performed CDISC mapping for clinical trial data such as Demographics (DM), Disposition (DS), Medical History (MH), Adverse Event (AE) table etc.

Generated Reports, Tables, Listings as per client’s approval based on the requirements generated using Base SAS Reporting Procedures. Developed complex SAS/Macros to simplify SAS code and effectively reduce coding time.

Tested and debugging existing MACROS.

(Sathish.K)

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