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Sr Stat Programmer

Iqvia
IQVIA
7-8 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

Senior Statistical Programmer

Location: Bangalore, India
Job Type: Full-Time
Application Deadline: January 24, 2026
Experience Required: 7–8+ years in statistical programming/clinical data analysis
Job ID: R1510905


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 combining advanced analytics, technology, and deep industry expertise. Our teams collaborate worldwide to deliver high-quality solutions that improve patient outcomes and support pharmaceutical and biotech clients in achieving their research goals.


Role Overview

The Senior Statistical Programmer provides advanced technical expertise and leadership to deliver integrated statistical programming solutions across complex clinical trials. This role supports both internal and external clients by planning, developing, and validating statistical programs, analysis datasets, and reporting tools, ensuring accuracy, efficiency, and compliance with regulatory and organizational standards.


Key Responsibilities

  • Plan, develop, and coordinate statistical programming for complex studies, including:

    • Programming, testing, and documenting statistical programs for tables, listings, and figures.

    • Creating and validating analysis datasets (derived datasets) and managing data transfers for clients.

  • Integrate databases from multiple studies or sources, ensuring data integrity and compliance.

  • Develop and maintain detailed programming documentation, specifications, and plans.

  • Provide advanced technical guidance and independent solutions for complex client requirements.

  • Develop, implement, and validate new process technologies, macros, and applications.

  • Lead statistical programming efforts for single or multiple complex studies, including budget and resource planning, scope management, and revenue forecasting.

  • Mentor and train junior programmers to enhance departmental capabilities.


Qualifications & Experience

  • Education:

    • Master’s degree in Computer Science or related field with 7 years relevant experience, or

    • Bachelor’s degree in Computer Science or related field with 8 years relevant experience, or

    • Equivalent combination of education, training, and experience.

  • Technical Skills:

    • Advanced expertise in Base SAS, SAS Graph, and SAS Macro Language.

    • Strong knowledge of statistics and clinical drug development processes.

  • Professional Skills:

    • Excellent organizational, leadership, interpersonal, and communication skills.

    • Ability to manage multiple tasks/projects effectively while ensuring high accuracy and attention to detail.

    • Ability to build and maintain effective working relationships with clients, managers, and team members.


Why Join IQVIA

  • Lead complex statistical programming projects for global clients.

  • Work with a world-class CRO and collaborate with cross-functional teams.

  • Opportunity to mentor and guide junior staff while advancing technical expertise.

  • Competitive compensation and growth opportunities in a globally recognized organization.


Apply Now via thepharmadaily.com to join IQVIA as a Senior Statistical Programmer and contribute to high-impact clinical research programs.