Senior Programmer FSP - RWD/EPI

Cytel; Jefferson City (MO); On-site; USD 110,000 - 170,000; Full time

Job summary

Cytel Inc. is seeking a data analytics professional to support Epidemiology by preparing Real World data and advising on analytic strategies.

You will program and conduct statistical analyses under supervision, linking datasets and creating analytical databases for observational studies. The role involves data standardization, visualization, and reporting, with collaboration across Medical Affairs, Global Patient Safety, and Clinical Development.

Qualifications

• Master’s degree or PhD in epidemiology, biostatistics, statistics, bioinformatics, or economics.
• 5+ years of experience conducting RWE analytics for pharma industry, CRO, or academic institution.
• Intermediate to expert SQL proficiency; SAS or R proficiency required.
• Deep expertise analyzing RWE data sources such as Optum Clinformatics Datamart, Truveta, UK Biobank.
• Familiarity with relational databases and claims data layouts.
• Experience with regression, survival, and propensity weighting analyses.

Responsibilities

• Provide support to the Epidemiology team by preparing Real World data and advising on analytic strategies.
• Program and conduct statistical analyses under supervision of epidemiologists/statisticians.
• Support data standardization, visualization, and reporting of observational data.
• Support Medical Affairs, Global Patient Safety/Risk Management, and Clinical Development activities.
• Partner with epidemiologists to manage relationships with internal and external stakeholders.
• Prioritize work across multiple projects and communicate clearly to ensure timely delivery.

Skills

SQL

SAS

R

Data analysis

Education

Master’s degree or PhD in related field

Job description

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 required
• 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

Cytel Inc. is an Equal Employment / Affir…