Principal Programmer - RWD/EPI

Cytel; Carson City (NV); Sur place; USD 120 000 - 180 000; Plein temps

Résumé du poste

Cytel is seeking a senior epidemiology/RWE analytics professional to join our team. You will work with epidemiologists to prepare RWD, advise on analytic approaches, and support stakeholder priorities across regulatory and clinical development activities.

Key responsibilities include data extraction, analysis, visualization, and reporting, with emphasis on collaboration and timely delivery. Strong SQL, SAS or R, and experience with major RWE sources are required.

Qualifications

• Master’s or PhD in epidemiology, biostatistics, statistics, bioinformatics, or related field with 5+ years of RWE analytics experience in pharma, CRO, or academia.
• Proficiency in SQL is required; SAS or R proficiency is required.
• Experience analyzing RWE sources such as Optum Clinformatics Datamart, Truveta, and UK Biobank is highly desirable.
• Strong foundation in relational databases and exposure to claims and ancillary file layouts.
• Experience with regression methods (OLS, longitudinal, logistic, Cox, GLM/GEE) and propensity weighting.
• Excellent project management skills with the ability to prioritize multiple tasks and stakeholders.
• Strong written and verbal communication for presenting evidence to internal and external audiences.

Responsabilités

• Provide support to the Epidemiology team by preparing Real World data and advising on analytic strategies.
• Program and conduct statistical analyses including data coding, algorithm development, and data linkage.
• Support data standardization, visualization, and reporting of observational data.
• Assist Medical Affairs, Global Safety, and Clinical Development through observational studies and regulatory safety documents.
• Partner with Epidemiologists to manage relationships with stakeholders.
• Prioritize and manage work across multiple projects.
• Communicate clearly to ensure timely project delivery and solve technical problems.

Connaissances

SQL

SAS

R

Data visualization

Communication

Applied statistics

Formation

Master’s degree

PhD

Outils

Optum Clinformatics Datamart

Market Clarity

Truveta

UK Biobank

Description du poste

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), surrogate 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 / Aff…? Applicants are considered for all positions without regard to race, color, religion, sex, national origin, age, veteran status, disability, sexual orientation, gender identity or expression, or any other characteristics protected by law.