Senior Data Analyst, CPRD

RWE Senior Data Analyst – CPRD

Job Overview

Real world evidence (RWE) has become a vital complement to the traditional clinical trial in the demonstration of the value and safety of new medicines. This senior data analyst role sits within our Real-World Solutions team and will be responsible for leading analyses for observational studies under one client portfolio. It is important for this individual to have training in observational research and the Clinical Practice Research Datalink (CPRD), 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

• Conduct analyses and determine methodological considerations (e.g., treatment patterns) for longitudinal studies using CPRD data and other secondary real world data sources, including claims and EHR 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
• Plan and program the integration/linkage of raw CPRD data (Gold and Aurum) to multiple RWD data sources
• Conduct QC programming for descriptive and complex studies in RWD
• Manage and contribute to quality control of programs and automation of data refreshes
• Support development of study documents including protocols, analysis specifications, and study reports with translation to analytic implementation
• 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
• Closely collaborate with epidemiologists and data scientists to develop and refine data management and analytic procedures, code lists, and workflows 

Qualifications

• Master's Degree in Biostatistics, Epidemiology, Data Science, or related field with 5-8 years relevant experience or PhD with 2 years of relevant experience required
• Knowledge of statistics, programming, and real-world studies
• Formal training and demonstrated proficiency in statistical programming using SAS, macros, basic SQL required
• Prior programming experience using Clinical Practice Research Datalink (CPRD) data required
• Strong track record of analysis of RWD
• Experience in inflammation and virology therapeutic areas a plus
• Good organizational, interpersonal, and communication skills
• Ability to effectively manage and prioritize multiple tasks and projects
• Excellent accuracy and attention to detail

Location

• Home-based anywhere in the United States or Canada.
• Relocation and work sponsorship not supported for this opening

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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

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

The potential base pay range for this role, when annualized, is $106,200.00 - $177,000.00. 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.