Senior Statistical Programmer
Job ID: R1510739
Location: Thane, India
Employment Type: Full-Time
Work Model: Hybrid
Industry: Clinical Research / Life Sciences
Experience Required: Minimum 8 Years
Job Overview
IQVIA is seeking an experienced Senior Statistical Programmer to provide advanced technical leadership and statistical programming expertise across complex clinical research studies. This role is responsible for designing and delivering integrated programming solutions that support the full spectrum of statistical analysis needs for internal teams and external clients. The position also plays a key role in process optimization, technical innovation, and team mentorship within a global clinical research environment.
Key Responsibilities
Lead and coordinate statistical programming activities for complex clinical studies, including programming, testing, and documentation of tables, figures, and listings (TFLs)
Develop and maintain analysis datasets, derived databases, and data transfers for internal and external stakeholders
Plan and execute database integration across multiple studies or data sources
Design and review programming plans, specifications, and documentation for complex projects
Provide advanced technical consultation to project teams and clients, delivering innovative programming solutions
Develop, implement, validate, and optimize new programming tools, macros, applications, and process technologies
Serve as Statistical Programming Lead for single complex studies or groups of studies
Manage scope of work, budget assumptions, effort estimates, and out-of-scope activities for assigned studies
Support project planning through accurate resource forecasting and revenue estimates
Ensure high-quality deliverables through rigorous quality control and validation processes
Provide technical training, guidance, and mentorship to junior and mid-level programmers
Collaborate effectively with cross-functional teams to ensure timely and compliant project delivery
Required Qualifications
Master’s degree in Computer Science, Statistics, or a related field with a minimum of 8 years of relevant experience, or
Bachelor’s degree in Computer Science, Statistics, or a related field with a minimum of 8 years of relevant experience, or
Equivalent combination of education, training, and experience in lieu of a formal degree
Strong understanding of statistical concepts, clinical trial processes, and drug development lifecycle
Advanced expertise in Base SAS, SAS Macro Language, and SAS Graph
Proven experience delivering statistical programming solutions in a regulated clinical research environment
Strong organizational, leadership, interpersonal, and communication skills
Demonstrated ability to manage multiple complex projects simultaneously
Exceptional attention to detail, accuracy, and quality standards
Ability to build and maintain effective working relationships with internal teams and external clients
About IQVIA
IQVIA is a global leader in clinical research services, healthcare intelligence, and commercial insights for the life sciences industry. By combining data, technology, and scientific expertise, IQVIA accelerates the development and commercialization of innovative medical treatments that improve patient outcomes and population health worldwide.
Equal Opportunity Employer
IQVIA is an equal opportunity employer. All qualified applicants will receive consideration for employment without discrimination based on race, religion, gender, age, disability, or any other legally protected characteristic.
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