Senior RWE/RWA Programmer

🕒 Junho 19

🇺🇸 Estados Unidos – Remoto (EUA)

⏰ Tempo Integral

🟠 Sênior

🖥 Engenheiro de Software

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Parexel

SiteLinkedInTodas as Vagas

10.000+ funcionários

Fundada em 1983

💼 Consultoria

🏥 Saúde

📦 Logística

💰 Venture Round em 1990-01

Consulting • Healthcare • Logistics

Parexel é uma das maiores organizações de pesquisa clínica (CROs) do mundo, oferecendo serviços abrangentes para o processo de desenvolvimento clínico das Fases I a IV. A empresa é especializada em gestão de portfólio, gestão de ensaios clínicos, estratégia regulatória, acesso ao mercado e gestão do ciclo de vida para biofarmacêuticos. A Parexel busca acelerar a chegada de medicamentos que transformam vidas ao mercado, alavancando sua expertise clínica, regulatória e terapêutica. Com uma equipe global de mais de 21. 000 profissionais, a Parexel trabalha para integrar insights de pacientes e desenhos de estudo inovadores a fim de desenvolver tratamentos em áreas terapêuticas como oncologia, neurociência, doenças raras, entre outras. Seu foco está na condução de ensaios clínicos eficientes e centrados no paciente.

Descrição

• Effectively designs and codes R and SQL programs for assigned project(s), consistently meeting project objectives • Clean and validate Real-World Data (RWD) to ensure consistency and reliability • Implement programming based on RWE protocols using a variety of RWD sources, including Optum and Flatiron • Leverage advanced statistical and epidemiological methodologies to deliver robust and reliable analyses • Create, review, and approve programming plans at both study and project levels • Demonstrate advanced knowledge of programming, epidemiological methodology implementation, and system development life cycle concepts • Maintain clear documentation of analytical programming and operational definitions to support reproducible and auditable RWE studies • Develop dashboards, reports, and presentations to effectively communicate findings • Collaborate with study team members to meet study timelines and recurring reporting deadlines

🎯 Requisitos

• MS in data science, epidemiology, statistics, public health, or related discipline • At least 7 years of experience in Real-World Data (RWD) analysis and Real-World Analytics (RWA) using healthcare claims, EMR, and/or registry databases within the biopharmaceutical industry or provider/payer organizations • Includes strong hands-on experience with Optum and/or Flatiron data • Fluency in SQL and R programming is required • Experience writing original code and performing raw data analysis (not derived solely from clinical trials) • Includes running analyses and/or developing code for real-world analyses • Knowledge of SAS and/or Python is considered an advantage • Familiarity with US and global healthcare coding systems (e.g., ICD, CPT, HCPCS, LOINC, MedDRA) And healthcare delivery systems (e.g., payers and reimbursement models) • Experience conducting routine and advanced statistical analyses for RWE generation Including time-to-event, cross-sectional, and longitudinal data • Experience with big data analytical platforms • Deep understanding of observational study analysis • Ability to work independently and contribute to scrum development goals In a fast-paced, flexible, team-oriented environment • Strong communication and collaboration skills • Competent in written and oral English.

🏖️ Benefícios

• Health insurance • 401(k) matching • Flexible work hours • Paid time off • Professional development opportunities