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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