Bachelor's degree from reputable university preferably in science/ mathematics related fields
Preferred SAS\xc2\xae certification
Technical Skills Requirements
Must have expertise of SAS\xc2\xae Base, and good knowledge of
SAS\xc2\xae graph and SAS\xc2\xae Macros.
Capable of implementing more advanced 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 8+ 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;
Perform all responsibilities associated with the Senior
Programmer role.
Assist all the Sr. Programmers and Programmers in their
day to day activities.
Act as escalation point for Sr. Programmer and
Programmer.
Regularly communicates with the sponsor on the progress
of programming aspects of the project and proactively anticipates issues and works with the sponsor on resolution of the problems
Provide input and/or write the programming specifications
Serve as subject matter expert on all aspects of SAS
programming
Understand pharmaceutical industry standards and trends
and proactively plan, develop, and implement
Develop consistent practices of clinical and statistical
review of output and mentor programming staff
Check for consistency across therapeutic areas
Identify, plan, and oversee the implementation and success
measures of all process improvement initiatives
Maintain expertise in the use of the SAS\xc2\xae Macros and
determine macro development priorities
Other responsibilities as defined on ad-hoc basis by senior
management.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