IQVIA is hiring to expand our dedicated Real World Evidence (RWE) FSP team, working fully within the environment of a prominent Pharma company. This senior data analyst role sits within our Real World Solutions team and will be responsible for leading development of datasets and conducting longitudinal analyses for observational studies in the virology therapeutic area under one client portfolio. It is important for this individual to have prior experience in observational research utilizing EMR and claims data, a strong statistical programming skillset, and experience managing multiple studies and complex analyses. In this role, individuals 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).

Essential Functions

• 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 (e.g. Optum, HealthVerity, TriNetX)
• 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 (e.g. longitudinal analysis, survival analysis, regression models) in studies using RWD for virology 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

Qualifications

• Master's Degree in Biostatistics, Epidemiology, Data Science or related field with 5-8 years relevant experience or PhD with 3 years relevant experience required
• Strong track record of analysis of RWD using EMR and claims data
• Experience analyzing TriNetX RWD is preferred
• Demonstrated proficiency in advanced statistical programming using SAS and/or R, macros, SQL required
• Prior pharmaceutical experience and advanced knowledge of observational research study design and analytic methodologies
• Experience in CRO/consultation with client engagement responsibilities
• Excellent analytic and communication skills with attention to detail
• Ability to effectively manage and prioritize multiple tasks and projects

This role is not eligible for UK visa sponsorship

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com