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Senior Statistical Programmer, Data Visualization

4+ years
$88,300 – $220,900,
10 Nov. 21, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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 – Data Visualization (Home-Based, U.S. or Canada)

Location: Durham, North Carolina (Home-Based Across U.S. or Canada)
Job Type: Full-Time
Job ID: R1509056

IQVIA is seeking an experienced Senior Statistical Programmer – Data Visualization to support a sponsor-dedicated team working within the environment of a leading global pharmaceutical organization. This fully remote role focuses on statistical programming, clinical data visualization, and real-time data review for ongoing clinical trials.

Role Overview

As a Senior Statistical Programmer, you will collaborate closely with clinical, biostatistics, and data management teams to deliver high-quality visual analytics and statistical outputs. You will support safety data visualization, dataset creation, and ongoing improvements to the programming environment using SAS, Spotfire, R, and other analytical tools.


Key Responsibilities

Statistical Programming & Data Visualization

  • Develop visualization-ready analysis datasets using SAS.

  • Build and maintain interactive data visualizations using Spotfire, R, and related tools.

  • Support real-time, online clinical trial data review and safety monitoring.

Data Quality & Analysis

  • Evaluate analysis data quality across studies.

  • Conduct cross-study analyses and ensure consistency with industry standards.

  • Support SDTM and ADaM specification creation and updates.

Collaboration & Documentation

  • Work closely with Clinical Development, Biostatistics, Clinical Data Management, and Global Drug Safety teams.

  • Participate in Programming and Biometrics meetings.

  • Assist in reviewing SOPs, policies, and controlled documents.

  • Follow established workflows for study setup within Spotfire and related systems.

Process Improvement

  • Contribute to continuous enhancements of the programming framework, tools, and operational efficiency.


Required Experience & Qualifications

  • Minimum 4+ years of industry experience in statistical programming within clinical research or life sciences.

  • Bachelor’s degree in Biostatistics, Computer Science, Biology, Pharmacology, or a related field.

  • Strong proficiency in SAS programming.

  • Advanced experience in data visualization, preferably with Spotfire.

  • Solid understanding of clinical trial design, safety analytics, and electronic data submission standards.

  • Ability to interpret programming specifications and follow analysis plans.

  • Experience in SQL, Python, or Java is an added advantage.


Why Join IQVIA?

IQVIA is a global leader in clinical research and healthcare data science. By joining this team, you will support the development of innovative therapies and contribute to data-driven insights that advance global patient care.


Compensation

Annualized Base Pay Range:
$88,300 – $220,900, based on experience, education, skills, location, and schedule.
Additional performance incentives, bonuses, and comprehensive health and welfare benefits may be available.

IQVIA is an equal opportunity employer and welcomes applicants regardless of race, color, religion, gender, sexual orientation, gender identity, national origin, disability, or protected veteran status.