Senior Epidemiological Programmer, Real World Evidence FSP

IQVIA is hiring to expand our dedicated Real World Evidence (RWE) FSP team working fully within the environment of a prominent Pharma company. Epidemiological Programmer 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 demonstrated experience and applied proficiency in observational research utilizing EMR and claims data a strong statistical programming skillset both knowledge and applied experience with epidemiological study design terminology cohort building and RWE outcome measures and experience managing multiple studies and complex this role individuals will have access to real-world databases and act as the stewards of the clients 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 IQVIA PharMetrics Plus)
• 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 censored data confounding differing person-time and missing data
• Collaborate with epidemiologists on study design and methodology as well as define specifications for descriptive and complex statistics (e.g. longitudinal analysis survival analysis regression models propensity score methods) 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 statistical and epidemiological expertise and independently bring project solutions to team for complex studies

Qualifications

• Masters Degree in Biostatistics Epidemiology Outcomes Research 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
• Demonstrated proficiency in advanced statistical programming using SAS and/or R macros SQL required
• Demonstrated experience and applied proficiency of RWE study design terminology cohort building and analytic methodologies
• Prior pharmaceutical or CRO experience
• Excellent analytic and communication skills with attention to detail
• Ability to effectively manage and prioritize multiple tasks and projects

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 .

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