3 days ago
Remote, United StatesSenior
Responsibilities
- Implement data and analysis infrastructure platforms and technical solutions supporting data flow from collection to submission.
- Develop reusable and robust R package code, utilities, processes, and tools.
- Create data analysis and visualization solutions for clinical data environments, including static outputs and dashboards.
- Gather and prioritize requirements for fit-for-purpose technical solutions.
- Collaborate with internal teams and study teams to improve quality, efficiency, processes, and tools.
- Provide detailed documentation and training and facilitate change management for department systems and processes.
Requirements
- At least 5 years of industry experience in pharma, biotech, or CRO environments.
- Experience using R in regulated clinical development environments.
- Strong R data manipulation and analysis skills using standard tidyverse packages.
- Strong R visualization skills for static outputs and dashboards.
- Experience developing R packages with appropriate documentation and testing.
- Experience developing SAS code, including SAS/MACRO, preferred.
- Familiarity with Posit Workbench, Positron, and Connect.
- Familiarity with the drug development life cycle and clinical trial data manipulation, analysis, and reporting.
- Ability to manage multiple competing priorities and work effectively with globally dispersed, cross-cultural teams.
Tech Stack
RSass
Categories
Data Engineering
About Cytel
Cytel builds clinical-trial design and analytics software and provides biometrics and data-science CRO services for biopharma and medical researchers. Its offerings include adaptive design tools like the East platform, along with statistical programming, data management, and regulatory support delivered via sponsor-dedicated teams. Founded in 1987 and headquartered in Cambridge, MA, Cytel is privately held and backed by Nordic Capital, with a global client base across pharmaceutical and biotechnology markets.