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.
How to Apply
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