ClinChoice Benefits Overview

Lead analytical efforts in Real World Data research, develop specifications and methodologies, manage projects, and communicate findings to stakeholders.

The Senior Statistical Programmer will program and validate datasets for clinical trials, oversee deliverables, manage projects, and ensure compliance with industry standards. Requires strong skills in SAS and R for statistical programming.

Lead and deliver clinical trial data management activities including database setup, eCRF specification, edit checks, testing, data review/reconciliation, database lock/unlock, SAE reconciliation, vendor/data transfers, team training, and oversight to ensure timelines and quality.