Statistical Programmer (Medical Device)

2 years

$88,300 – $220,900

Washington

10 Sept. 9, 2025

Job Description

Job Type: Full Time Education: B.Sc/M.Sc/ B.Pharma/ M.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

Job Title:

Statistical Programmer (Medical Device)
📍 Washington, DC (Home-based)
🕒 Full-Time
📄 Job ID: R1487403
🌍 Job available in additional locations

Company Overview

IQVIA is a global leader providing clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We accelerate the development and commercialization of innovative medical treatments to improve patient outcomes worldwide.

🌐 Learn more: https://jobs.iqvia.com

Job Overview

Provide advanced technical expertise in statistical programming to develop and implement integrated programming solutions that meet internal and external client needs. Lead programming efforts on complex studies, including database integration, quality control, and documentation. Serve as a consultant on project requirements and contribute to process improvements and training.

Essential Functions

Plan, coordinate, and execute programming, testing, and documentation of statistical programs for tables, figures, and listings.
Program and manage analysis databases (derived datasets) and data transfers for internal and external clients.
Integrate databases from multiple studies or sources.
Develop and coordinate programming documentation including plans and specifications for complex studies.
Provide advanced technical expertise and independently develop project solutions.
Develop, implement, and validate new process technologies, macros, and applications.
Lead statistical programming teams for complex single studies or study groups.
Understand project scope, budget, and quote assumptions; estimate work completed and manage out-of-scope and resource forecasts.
Manage project budgets, resource requirements, and provide revenue forecasts as needed.
Provide training and guidance to junior staff.

Qualifications

Education & Experience

Master’s Degree in Computer Science or related field with 3 years relevant experience
OR
Bachelor’s Degree in Computer Science or related field with 4 years relevant experience
Equivalent combination of education, training, and experience considered
Medical device experience preferred
SAS Certification preferred

Skills & Knowledge

Strong knowledge of clinical research and statistical data standards, including CDISC SDTM, ADaM, and ICH Statistical Principles for Clinical Trials
Advanced proficiency in Base SAS, SAS Graph, and SAS Macro Language
Knowledge of statistics, programming, and clinical drug development processes
Excellent organizational, interpersonal, leadership, and communication skills
Strong multitasking and project management abilities
Exceptional accuracy and attention to detail
Ability to build and maintain effective working relationships with colleagues, management, and clients

Compensation & Benefits

💰 Annual Salary Range:
$88,300 – $220,900 (depending on qualifications, experience, and location)

Additional benefits may include:

Incentive plans
Bonuses
Health and welfare programs

Work Environment

🏠 Home-based/Remote

Equal Employment Opportunity

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or other protected statuses.

🔗 EEO Policy

How to Apply

🔗 Apply Now

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Statistical Programmer (Medical Device)

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