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Assoc. Sr. Stat Programmer

Iqvia
IQVIA
3-7 years
Not Disclosed
10 Jan. 22, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

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.