CDM Programmer II ( SAS )
Core
CDM Programmer II responsible for database development, data validations, and listing creation using SAS within clinical data management systems.
Role type
mid-level individual contributor CDM programmer
Builds
clinical trial data listings, data transfers, and reconciliation reports
Domain
pharmaceuticals / clinical data management
Required skills
SAS programming, SQL, data validation, listing development, data extraction from EDC systems, GCP compliance, technical problem resolution, project management
Preferred skills
mentoring junior programmers, process improvement, reporting tool creation, system troubleshooting
Technologies
SAS, SQL, Crystal Reports, JReview, EDC systems
Responsibilities
Define and import data into systems; create and test listings for data review; perform data transfers based on standards; generate reconciliation listings and specialized reports (patient profiles, MPRs, SSTs, SAE reconciliation); research and resolve technical issues; train and mentor junior programmers; contribute to reporting tools and process initiatives.
Seniority
Mid-level, hands-on IC with technical leadership