Job Description

Bachelor's degree from reputable university preferably in


science/ mathematics related fields


Preferred SAS certification
Technical Skills


Requirements


Must have expertise of SAS Base, and good knowledge of
SAS graph and SAS 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 Macros and
determine macro development priorities


Other responsibilities as defined on ad-hoc basis by senior
management.


Relationship & Interactions


Clinical data manager Biostatisticians Medical Coders IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at https://jobs.iqvia.com