
51 - 200 employees
💼 Consulting
🏥 Healthcare
🧬 Biotechnology
Consulting • Healthcare • Biotechnology
Clinical Outcomes Solutions is a global clinical outcomes consultancy that provides comprehensive support and services in all aspects of Clinical Outcome Assessment (COA) research. The company helps inform patient care by capturing the patient voice through innovative scientific methods. It guides organizations in navigating the complexities of clinical outcomes research by crafting strategies and solutions to capture accurate data. Trusted by pharmaceutical and biotechnology companies, the firm ensures regulatory compliance and optimized patient outcomes.
🕒 July 16
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51 - 200 employees
💼 Consulting
🏥 Healthcare
🧬 Biotechnology
Consulting • Healthcare • Biotechnology
Clinical Outcomes Solutions is a global clinical outcomes consultancy that provides comprehensive support and services in all aspects of Clinical Outcome Assessment (COA) research. The company helps inform patient care by capturing the patient voice through innovative scientific methods. It guides organizations in navigating the complexities of clinical outcomes research by crafting strategies and solutions to capture accurate data. Trusted by pharmaceutical and biotechnology companies, the firm ensures regulatory compliance and optimized patient outcomes.
• Implement the vision for data and analysis infrastructure platforms and other technical solutions supporting data flow from data collection to data submission • Use R programming and clinical-trial expertise to create solutions enabling an open-source programming ecosystem • Coordinate gathering and prioritizing requirements for designing and delivering fit-for-purpose data and analysis technical solutions • Collaborate with internal teams to understand requirements and develop processes, tools, and utilities that improve quality and efficiency • Develop reusable and robust R package code and/or utilities with detailed training and documentation • Promote technical innovation for data analysis and visualization solutions within a clinical data environment • Partner with study teams to use and further improve processes and tools • Facilitate change-management activities and training for department systems and processes
• 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
Apply Now🕒 July 16
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