Associate Senior Statistical Programmer
Location: Bangalore, India
Job Type: Full-Time
Application Deadline: January 24, 2026
Experience Required: 3–7 years in statistical programming/clinical data analysis
Job ID: R1517432
Company Overview
IQVIA is a global leader in clinical research, healthcare intelligence, and life sciences solutions. We accelerate the development and commercialization of innovative medical treatments by leveraging advanced analytics, technology, and domain expertise. Our teams deliver high-quality solutions that improve patient outcomes while supporting pharmaceutical and biotech clients worldwide.
Role Overview
The Associate Senior Statistical Programmer plays a key role in developing and implementing software solutions for the statistical analysis of clinical trial data. This role works closely with statisticians, data managers, and project stakeholders to ensure data integrity, regulatory compliance, and timely delivery of high-quality programming outputs across multiple clinical research projects.
Key Responsibilities
Develop, test, and implement software solutions to support statistical analysis of clinical trial data.
Collaborate with statisticians and project teams to ensure accurate, efficient, and compliant data processing.
Apply statistical methods and programming techniques across multiple clinical research projects.
Utilize statistical programming languages (SAS, R) and software tools to optimize data analysis workflows.
Conduct quality control and ensure all programming deliverables meet regulatory and company standards.
Troubleshoot programming issues, interpret complex datasets, and provide actionable insights to support clinical decisions.
Mentor and provide guidance to junior programmers and team members.
Manage multiple programming tasks and ensure deadlines are consistently met.
Qualifications & Experience
Education: Bachelor’s Degree in Statistical Programming, Computer Science, or a related field.
Technical Skills:
Proficiency in SAS, R, or other statistical programming languages.
Strong analytical skills to evaluate statistical results and troubleshoot programming issues.
Professional Skills:
Experience collaborating with statisticians, data managers, and project managers.
Ability to manage multiple programming projects simultaneously.
Attention to detail and commitment to quality and regulatory compliance.
Why Join IQVIA
Work on high-impact clinical research projects with global exposure.
Collaborate with cross-functional teams in a world-class CRO environment.
Gain opportunities for mentorship, professional development, and career growth.
Contribute to the development of innovative solutions that improve patient outcomes globally.
Apply Now via thepharmadaily.com to join IQVIA as an Associate Senior Statistical Programmer and advance your career in clinical data science and statistical programming.
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