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
