Senior Statistical Programming Analyst, Inflammation, Real World Evidence - FSP (Sponsor – Dedi[...] in Reading

Join IQVIA’s Sponsor-Dedicated FSP team and help advance healthcare through real-world evidence. We bring together scientific expertise and real-world data to help sponsors make decisions and accelerate evidence generation to improve patient outcomes. In this role, you’ll work closely with one sponsor, gaining deep knowledge of their therapies while leveraging IQVIA’s global expertise. You’ll be part of a collaborative team that values your contribution, supports your growth, and helps shape the future of evidence generation and your career.

Overview

As a Senior Data Analyst, you will be responsible for leading the development of datasets and conducting longitudinal analyses for observational studies in inflammation under one client portfolio. You will have prior experience in observational research, utilising HealthVerity healthcare data, strong statistical programming skillset, and experience managing multiple studies and complex analyses. In this role, you will have access to real-world databases and act as the stewards of the client’s best practices, standards, and methodologies underlying the use of real-world data (RWD).

Responsibilities

• Lead development of analytic datasets through raw data processing and conduct data checks / cleaning using secondary real world data sources, including claims, EHR, and lab data.
• Lead the feasibility of real-world data sources to characterize patient population, build patient cohorts, and define and validate key variables specific to study objectives.
• Conduct and QC analyses, including identification of diagnosis and treatment codes and applying statistical methods to handle sensor data, confounding, and missing data.
• Collaborate with epidemiologists to define specifications for descriptive and complex statistics in studies using RWD for inflammation research questions.
• Develop and QC TFLs for protocols/reports/manuscripts using RWD (e.g. claims and EHR).
• Support development of other study documents including protocols, statistical analysis plans, and study reports.
• Communicate timelines, progress reports, and results to project team and key stakeholders.
• Provide technical, programming, and statistical expertise and independently bring project solutions to team for complex studies.

Requirements

• PhD in Biostatistics, Epidemiology, Data Science or related field with 3 years relevant experience or Master's Degree with 5-8 years relevant experience required.
• Knowledge of statistical methods, programming, and real-world studies.
• Prior programming experience using HealthVerity healthcare data.
• Formal training and demonstrated proficiency in statistical programming using SAS, macros, basic SQL required.
• Experience in CRO/consultation with client engagement responsibilities.
• Strong track record of analysis of RWD using claims and EHR data.

What’s in it for you?

Be part of a forward-thinking team that helps shape the next generation of evidence-based healthcare. Work hand-in-hand with one leading sponsor, gaining deep expertise in their therapies. Access IQVIA’s global network who supports your growth. This is your chance to make an impact, while building a career that matters.