Senior Epidemiological Programmer, Real World Evidence - FSP

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

• Master's 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

Additional information

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.

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Pay and benefits

The potential base pay range for this role, when annualized, is $88,300.00 - $220,900.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.