Senior Stat Programmer

IQVIA LLC; Hyderabad; On-site; INR 1,500,000 - 2,100,000; Full time

Job summary

IQVIA Hyderabad is seeking a Senior Stat Programmer to develop and coordinate programming solutions for complex studies, including statistical tables, figures, and listings. You will lead technical work, validate processes, and mentor junior staff while collaborating with clients and internal teams across the clinical development lifecycle.

A Master’s or Bachelor’s degree in computer science or a related field with strong SAS expertise is required.

Qualifications

• Knowledge of statistics, programming and the clinical drug development process.
• Advanced knowledge of SAS tools: Base SAS, SAS Graph and SAS Macro Language.
• Strong organizational, interpersonal, leadership and communication skills.

Responsibilities

• Program, test, and document statistical programs for tables, figures, and listings.
• Plan integration of databases from multiple studies or sources and develop programming documentation.
• Provide advanced technical expertise and leadership to teams and clients on complex studies.

Skills

Statistical programming

Leadership

Communication

Project coordination

Education

Master’s Degree in Computer Science or related field

Bachelor’s Degree in Computer Science or related field

Tools

Base SAS

SAS Graph

SAS Macro Language

Job description

## Senior Stat ProgrammerApplylocations: Hyderabad, Telangana, Indiatime type: Full timeposted on: Posted Todaytime left to apply: End Date: June 26, 2026 (22 hours left to apply)job requisition id: R1546778Job Overview Provide experienced technical expertise to develop process methodology for department to meet internal and external clients’ needs. Plan and coordinate the development of integrated programming solutions serving the full spectrum of statistical programming needs. Provide technical expertise and leadership to the department. Provide internal consulting services, including specifications and user needs analysis for complex project or client requirements.Essential Functions • Perform, plan and co-ordinate the following for complex studies: (i) the programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, and listing summaries and (ii) the programming of analysis databases (derived datasets) and transfers of data for internal and external clients. May perform and plan the programming of database quality control checks. • Program and plan the integration of databases from multiple studies or sources. • Develop and co-ordinate programming documentation including plans and specifications, as appropriate, for complex studies. • Provide advanced technical expertise in conjunction with internal and external clients, and independently bring project solutions to teams and department, for complex studies. • Perform, plan and co-ordinate the development, implementation and validation of new process technologies, macros and applications. • Fulfill project responsibilities at the level of statstical team lead for single complex studies or group of studies. • Understand the Scope of Work, budget and quote assumptions, estimate the work completed, manage Out of Scope and resource forecasts for single studies. May manage project budget and resource requirements, and provide revenue forecasts for single studies. • Provide training and guidance to lower level staff.Qualifications • Master's Degree Computer science or related field and 3 years relevant experience Req Or • Bachelor's Degree Computer science or related field and 4 years relevant experience Req • Equivalent combination of education, training and experience in lieu of degree Req • Knowledge of statistics, programming and/or clinical drug development process • Advanced knowledge of computing applications such as Base SAS, SAS Graph and SAS Macro Language • Good organizational, interpersonal, leadership and communication skills • Ability to effectively manage multiple tasks and projects • Excellent accuracy and attention to detail • Ability to establish and maintain effective working relationships with coworkers, managers and clientsIQVIA 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.comIQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.