Senior R Statistical Programmer

Emploi pas sur LinkedIn

🕒 il y a 25 jours

🇬🇧 Royaume-Uni – Télétravail

⏰ Temps Plein

🟠 Senior

🖥 Ingénieur Logiciel

🗣️🇺🇸🇬🇧 Anglais requis

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Logo of Clinical Outcomes Solutions

Clinical Outcomes Solutions

51 - 200 employés

💼 Conseil

🏥 Santé

🧬 Biotechnologie

Consulting • Healthcare • Biotechnology

Clinical Outcomes Solutions est un cabinet de conseil mondial en résultats cliniques qui offre un soutien et des services complets dans tous les aspects de la recherche sur l'évaluation des résultats cliniques (COA). L'entreprise aide à informer les soins aux patients en capturant la voix des patients grâce à des méthodes scientifiques innovantes. Elle guide les organisations dans la navigation des complexités de la recherche sur les résultats cliniques en élaborant des stratégies et des solutions pour capturer des données précises. Fiable pour les entreprises pharmaceutiques et biotechnologiques, la société garantit la conformité réglementaire et l'optimisation des résultats pour les patients.

Description

• Collaborates with internal teams to understand requirements and develop processes, tools and utilities that will improve quality and efficiency • Develops reusable and robust R package code and/or utilities, along with detailed training/documentation • Promotes technical innovation to drive the development of data analysis and visualization solutions within a clinical data environment • Partners with study teams in use and further improvement of processes and tools • Facilitates change management activities and training for department systems and processes

🎯 Exigences

• Minimum 5 years’ industry experience (Pharma, Biotech, CRO) • Experience with R within regulated clinical development environments • Strong R data manipulation and analysis skills using standard tidyverse packages • Strong R visualization skills for use in static outputs and dashboards • Experience with developing R packages including proper documentation and testing • Experience developing SAS code including SAS/MACRO preferred • Familiarity with Posit products including Workbench, Positron, and Connect • High attention to detail including proven ability to manage multiple, competing priorities • Familiarity with drug development life cycle and experience with manipulation, analysis, and reporting of clinical trials’ data • Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners

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