Job Description

ob Title Senior Statistical Programmer
Functional Area Statistical Programming
Education Requirements \xe2\x80\xa2 Bachelor\'s degree from reputable university preferably in
science/ mathematics related fields

• Attained SAS\xc2\xae certification

Technical Skills Requirements \xe2\x80\xa2 Must have excellent knowledge of SAS\xc2\xae Base, and good
knowledge of SAS\xc2\xae graph and SAS\xc2\xae 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 \xe2\x80\xa2 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\xc2\xae

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\xc2\xae 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 \xe2\x80\x93 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\xc2\xae 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 \xe2\x80\xa2 Clinical Data Manager

• Biostatisticians
• Medical Coders

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 \xe2\x80\x93 to help our customers create a healthier world. Learn more at

IQVIA