Statistical Programmer II

🕒 Junho 17

🌲 North Carolina, Texas – Remoto

🌲 North Carolina – Remote 🤠 Texas – Remote

💵 $90.000 - $100.000 / ano

⏰ Tempo Integral

🟡 Pleno

🟠 Sênior

🖥 Engenheiro de Software

🦅 Patrocina Visto H1B

Esta empresa já patrocinou vistos H1B no passado.

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LivaNova

SiteLinkedInTodas as Vagas

1001 - 5000 funcionários

🏭 Manufatura

🏥 Saúde

🧬 Biotecnologia

Manufacturing • Healthcare • Biotechnology

LivaNova PLC é uma empresa global de tecnologia médica, construída sobre quase cinco décadas de experiência e um compromisso incansável de melhorar a vida de pacientes em todo o mundo. Nossas tecnologias avançadas e tratamentos inovadores oferecem soluções significativas em benefício dos pacientes, dos profissionais de saúde e dos sistemas de saúde.

Descrição

• Support programming activities for multiple projects on clinical study reports and publications • Accountable for clinical statistical programming deliverables and for ensuring excellence in programming activities in terms of quality and timelines for clinical trials under the responsibility of Statistics & Data Management • Collaborate with Statistics, Data Management, Clinical, and vendor teams to clarify requirements and resolve data or programming issues • Develop, validate, and maintain SAS programs in accordance with study requirements, internal standards, and SOPs • Contribute to the creation, validation, and documentation of SDTM and ADaM datasets • Responsible for producing programming outputs, validation, and related documentation to ensure accuracy, consistency, and traceability • Ensure deliverables meet expectations in terms of timelines and quality, regulatory and key user group requirements (e.g., CDISC), operational efficiency, and alignment with the study's clinical and statistical objectives • Provide input into SAP, analysis specifications, and data presentations for clinical trials • Support ongoing workflow modernization, migration activities, and standardization initiatives • Participate in process improvement activities related to programming efficiency, quality, and standardization

🎯 Requisitos

• Bachelor’s degree or higher in statistics, mathematics, computer science, life sciences, data science, or related field • Relevant experience in clinical trial programming, clinical data analysis, statistical programming, or regulated data environments • Strong SAS programming skills, including data step, procedures, macros, and debugging • Ability to write clear, validated, reusable, and well-documented code • Understanding of programming quality control, validation, and traceability expectations • Working knowledge of CDISC standards, especially SDTM and ADaM • Ability to support dataset creation, validation, listings, tables, figures, and ad hoc analyses • Understanding of clinical trial data flow from data collection to analysis/reporting • Strong attention to detail and quality • Ability to work independently on assigned tasks with appropriate guidance • Good communication skills and ability to collaborate with Statistics, Data Management, Clinical, and external vendors • Ability to manage priorities and timelines in a changing project environment

🏖️ Benefícios

• Health benefits – Medical, Dental, Vision • Personal and Vacation Time • Retirement & Savings Plan (401K) • Employee Stock Purchase Plan • Training & Education Assistance • Bonus • Referral Program • Service Awards • Employee Recognition Program • Flexible Work Schedules