Principal Statistical Programmer – FSP, RWD/EPI

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🕒 Ontem

🗽 New York – Remoto

🗽 New York – Remote

⏰ Tempo Integral

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🖥 Engenheiro de Software

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Clinical Outcomes Solutions

SiteLinkedInTodas as Vagas

51 - 200 funcionários

🧬 Biotecnologia

💊 Farmacêutico

⚕️ Seguro de Saúde

Biotechnology • Pharmaceuticals • Healthcare Insurance

A Clinical Outcomes Solutions é uma consultoria global de desfechos clínicos que oferece suporte e serviços abrangentes em todos os aspectos da pesquisa de Avaliação de Desfecho Clínico (COA). A empresa ajuda a informar o cuidado ao paciente capturando a voz do paciente por meio de métodos científicos inovadores. Ela orienta as organizações a navegar nas complexidades da pesquisa de desfechos clínicos, elaborando estratégias e soluções para capturar dados precisos. Confiada por empresas farmacêuticas e biotecnológicas, a empresa garante conformidade regulatória e otimização dos resultados dos pacientes.

Descrição

• 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

🎯 Requisitos

• 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.