Principal Statistical Programmer FSP - RWD

In this role you will join our FSP team and will work in support of the Epidemiology team within our client, a top pharmaceutical company.

You will contribute by:

• Providing support to the Epidemiology team by preparing Real World data, advising on data analytic strategies, and supporting stakeholders in various epidemiology analytic activities.
• Programming and conducting statistical analysis under the direction and supervision of epidemiologists/statisticians including data coding, creation of algorithms, linkage of datasets, and use of statistical packages or platforms.
• Supporting statistical programming to generate innovative means of data standardization, visualization, and reporting of observational data.
• Supporting Medical Affairs (e.g. observational studies leveraging RWD); Global Patient Safety and Risk Management (e.g., analysis to obtain background rates) for the development of regulatory/safety documents, and Clinical Development (e.g.; assessment of patient populations/ protocol feasibility).
  • The position will partner with Epidemiologists to manage relationships with internal and external stakeholders.  
• Being able to prioritize and manage work across multiple projects and stakeholders.
• Providing strong communication to ensure successful and timely project delivery.  
• Solving technical problems with experience and expertise.

Summary of Key Responsibilities

• Assist in development of study protocols and analysis plans leveraging large RWD sources (Claims and/or EHR)
• Liaise with data vendors to obtain relevant data extracts for research studies consistent with study protocols
• Create analytical databases from data extracts to facilitate conduct of data analyses
• Conduct analyses consistent with methods set forth in study protocols and analysis plans
• Produce tables and figures for discussions with other investigators, clients, and for study reports
• Present results internally and to clients
• Assist in the preparation of study reports and other deliverables
• May have supervisory responsibilities in the future

What we’re looking for:

• Master’s degree or PhD in related field (epidemiology, biostatistics, statistics, bioinformatics, economics) and 5+ years of experience conducting RWE analytics for pharma industry, CRO, or academic institution.
• Intermediate to expert level proficiency in SQL is a must. In addition, SAS or R proficiency is required.
• Deep expertise analyzing RWE data sources such as Optum (Clinformatics Datamart® and Market Clarity), Truveta and UK Biobank. Experience analyzing clinical trial and/or registry data is desirable.
• Familiarity with relational databases and proficient understanding of claims and ancillary file layouts.
• Experience with applied statistics including regression analysis (OLS, longitudinal, logistic, Cox, GLM/GEE), survival analyses (Kaplan-Meier, cumulative incidence, accelerated failure time models), and propensity weighting.
• Excellent project management skills; can prioritize multiple tasks and goals to ensure timely completion.
• Confident and competent when interacting with internal and external stakeholders.
• Strong written/verbal communication skills. Highly effective at summarizing and presenting key considerations and evidence.