ClinChoice Benefits Overview

Lead and support clinical statistical programming: develop, validate, and maintain SAS programs; create SDTM/ADaM datasets and TLFs; collaborate with Biostatistics, Data Management, and Clinical teams; ensure deliverable quality and timelines; review specifications, participate in study planning, and support regulatory submission activities.

Develop and validate SDTM and ADaM datasets using R per CDISC standards, support TLF generation in R or SAS, perform QC and reconcile data issues, collaborate with biostatistics and clinical teams, and contribute to automation and reproducible workflows for regulatory submissions.

Lead statistical activities for oncology clinical trials, providing strategic input, developing analysis plans, and mentoring junior statisticians. Collaborate on regulatory submissions and ensure compliance with standards.