Assoc Sr Stat Programmer

2 weeks ago

Hyderabad, India IQVIA Full time

Senior Statistical Programmer
Functional Area Statistical Programming
Education Requirements • Bachelor's degree from reputable university preferably in 
science/ mathematics related fields
• Attained SAS® certification
Technical Skills Requirements • Must have excellent knowledge of SAS® Base, and good 
knowledge of SAS® graph and SAS® Macros.
• Capable of programming simple statistical procedures as per 
specifications provided by biostatistician.
• Must have excellent knowledge of CDISC standards (SDTM 
and ADaM)
• Thorough understanding of relational database components 
and theory.
• Excellent application development skills.
• Strong understanding of clinical trial data and extremely 
hands on in data manipulations, analysis and reporting of 
analysis results.
• Good understanding of ICH E6, ICH E3, ICH E8, ICH E9 and 
clinical research processes.
Experience Requirements Minimum of 5+ years of experience in Statistical Programming in 
pharmaceutical or medical devices industry
Desirable Requirements • Good verbal and written communication skills. 
• Ability to work on multiple projects, plan, organize and 
prioritize activities.
Responsibilities At a minimum, following activities are required to be performed:
• Adherence to all department-specific and project standards 
and SOPs 
• Perform all responsibilities associated with SAS® 
Programmer roles. 
• Assist the Programmers of their team in their day to day 
activities. 
• Act as an escalation point for Programmer. 
• Communicate with the sponsor as needed to ensure high 
quality and on time deliverables 
• Recommend and develop project standards 
• Apply SAS® programming knowledge to solve problems 
related to non-routine situations 
• Understand, own and author the programming 
specifications and database definitions 
• Generate and QC summary tables, data listings and graphs 
for in-house analyses of study data or publications using SAS 
standard coding practices. 
• Create/acquire tools to improve programming efficiency or 
quality Validate work of other programmers.
FILE 2
JOB DESCRIPTION – SENIOR STATISTICAL PROGRAMMER - IQVIA
• Create/review programming plan, specifications for 
datasets and TLFs. Conduct plausibility and completeness 
checks of programming output across each study. 
• Lead and own identified opportunities of process 
improvement 
• Identify, build and validate SAS® Macros 
• Contribute to activities in validation and implementation 
including Standard Reporting Systems, SAS macro utility 
programs and associated tools. 
• Contribute in development and implementation of 
programming standards and conventions. 
• Establish monitoring of data transfers for ongoing trials to 
identify study conduct or data quality issues. 
• Support data queries from other functional group 
• Other responsibilities as defined on ad-hoc basis by senior 
management.
Relationships & Interactions • Clinical Data Manager 
• Biostatisticians 
• Medical Coders
Report To IQVIA Associate Director/IQVIA Line Manage

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at

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