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