RWE Senior Data Analyst – Real World Evidence (Home-Based, U.S. or Additional Locations)
Location: Durham, North Carolina
Job Type: Full-Time
Job ID: R1513702
Work Model: Home-Based
IQVIA is expanding its Real World Evidence (RWE) Functional Service Provider (FSP) team and is seeking a highly experienced RWE Senior Data Analyst. This role operates fully within the environment of a leading global pharmaceutical client and supports observational research within the virology therapeutic area. The position is part of IQVIA’s Real World Solutions team and is ideal for professionals with advanced real-world data expertise and strong statistical programming capabilities.
Position Overview
The RWE Senior Data Analyst will lead dataset development, manage longitudinal analyses, and ensure high-quality delivery of observational research involving EMR, EHR, claims, and other real-world data sources. The role requires a strong technical foundation, experience executing complex study methodologies, and the ability to manage multiple analytical projects across a large client portfolio.
Key Responsibilities
Real-World Data Processing & Dataset Development
Lead the creation of analytic datasets from raw real-world data, including claims, EHR, and laboratory data sources such as Optum, HealthVerity, and TriNetX.
Perform data quality checks, cleaning, and validation to ensure accuracy and consistency.
Feasibility & Study Design Support
Evaluate RWD source feasibility to characterize patient populations and build patient cohorts.
Define and validate key variables aligned with study-specific objectives.
Advanced Statistical Analysis
Conduct and quality control statistical analyses, including coding identification, treatment patterns, survival models, longitudinal methods, and regression techniques.
Apply statistical approaches to address confounding, missing data, and sensor data challenges.
Cross-Functional Collaboration
Work closely with epidemiologists to define analytic specifications for complex statistical outputs.
Develop and QC TFLs (tables, figures, listings) for protocols, reports, and manuscripts using real-world datasets.
Study Documentation & Reporting
Support the development of protocols, statistical analysis plans, and final study reports.
Communicate analytical timelines, deliverables, and findings to internal teams and client stakeholders.
Technical Leadership
Provide expert-level programming, statistical, and methodological insights.
Independently propose solutions for analytical challenges in complex studies.
Required Experience & Qualifications
Master’s degree in Biostatistics, Epidemiology, Data Science, or related discipline with 5–8 years of relevant experience, or
PhD with 3+ years of relevant experience.
Demonstrated expertise in analyzing real-world data, including EMR and claims datasets.
Experience with TriNetX RWD preferred.
Strong proficiency in SAS, R, macros, and SQL.
Prior experience in pharmaceutical research, observational study design, and advanced analytic methodologies.
Background in CRO or consulting environments with client-facing responsibilities.
Excellent communication, analytical thinking, and organizational skills.
Ability to manage and prioritize multiple concurrent projects independently.
Why Join IQVIA?
IQVIA is a global leader in life sciences analytics, real-world evidence, and clinical research services. Joining this team means contributing to meaningful research that advances patient outcomes, supports innovation, and drives data-informed decisions in healthcare.
Compensation
Annualized Base Pay Range:
$88,300 – $220,900, depending on experience, skills, education, location, and work schedule.
Additional incentives, bonuses, and comprehensive health and welfare benefits may be offered based on the position.
IQVIA is an equal opportunity employer and welcomes applicants from all backgrounds without discrimination based on legally protected categories.
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