Remote Data Jobs · CDISC

• Develop, validate, and maintain SDTM and ADaM datasets using R following CDISC standards.
• Write efficient, reproducible, and well-structured R scripts for clinical data analysis and reporting.
• Perform QC checks, reconcile data issues, and ensure deliverables meet regulatory expectations.

• Lead programming activities for oncology clinical trials across multiple studies.
• Develop, validate, and maintain SDTM and ADaM datasets following CDISC guidelines.
• Prepare submission-ready programming outputs and documentation, including define.xml, annotated CRFs, and reviewer guides.

• Leads statistical programming activities for compounds/indications or a therapeutic area.
• Manages a team of statistical programmers and resource planning.
• Develops SAS programs for ADaM data sets and Tables, Listings, and Figures.

Take a leading role in programming and delivering complex clinical study datasets and statistical outputs for global pharmaceutical trials. Oversee SDTM, ADaM, and TLF development, ensuring high-quality results while mentoring junior team members. Work closely with cross-functional teams, coordinating programming activities, managing resources, and contributing to submissions. Attention to detail and strong technical expertise are key.

The Senior/Principal R Programmer Consultant will utilize advanced expertise in SAS, R, and Power BI to support clinical trial data analysis, reporting, and visualization. In this role, you will lead programming activities across multiple studies, ensuring high-quality and regulatory-compliant deliverables while enabling data-driven insights through interactive visualizations.