Senior Programmer – RWD/EPI

Vaga não está no LinkedIn

🕒 Agosto 21

🌐 Estados Unidos, Canadá – Remoto

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⏰ Tempo Integral

🟠 Sênior

🖥 Engenheiro de Software

🦅 Patrocina Visto H1B

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👻 Score fantasma 24%

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🗣️🇺🇸🇬🇧 Inglês obrigatório

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Logo of Clinical Outcomes Solutions

Clinical Outcomes Solutions

51 - 200 funcionários

💼 Consultoria

🏥 Saúde

🧬 Biotecnologia

Consulting • Healthcare • Biotechnology

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

• Provide support to the Epidemiology team by preparing Real World data, advising on data analytic strategies, and supporting stakeholders in epidemiology analytic activities • Program and conduct statistical analysis under the direction and supervision of epidemiologists/statisticians, including data coding, algorithm creation, dataset linkage, and use of statistical packages or platforms • Support statistical programming for data standardization, visualization, and reporting of observational data • Support Medical Affairs, Global Patient Safety and Risk Management, and Clinical Development activities involving RWD and observational studies • Partner with Epidemiologists to manage relationships with internal and external stakeholders • Prioritize and manage work across multiple projects and stakeholders • Provide strong communication for successful and timely project delivery • Solve technical problems using experience and expertise • Assist in developing study protocols and analysis plans leveraging large RWD sources (Claims and/or EHR) • Liaise with data vendors to obtain relevant data extracts • Create analytical databases from data extracts • Conduct analyses according to study protocols and analysis plans • Produce tables and figures for investigators, clients, and study reports • Present results internally and to clients • Assist in preparing study reports and other deliverables • May have supervisory responsibilities in the future

🎯 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 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

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