RAM Reporting Programmer II
Core
Develop and maintain clinical reports, listings, and data validation logic to support global clinical trials and ensure high-quality data outputs.
Role type
Senior IC clinical data reporting programmer
Builds
Clinical trial reports, listings, and validated data outputs for study teams
Domain
Clinical research / pharmaceutical data management
Deliverable
production ML models | product features | dashboards & analysis
Required skills
SQL, SAS, CQL, data validation, clinical reporting standards, data quality assurance, database development, data processing, data visualization, PL/SQL
Preferred skills
Pharmaceutical industry experience, external data integration experience, standardized reporting frameworks
Technologies
Veeva CDB, JReview, Cognos (InForm), Power BI
Responsibilities
Develop and maintain clinical reports and listings; Implement programmed data validation logic and discrepancy checks; Support reporting activities across the clinical trial lifecycle; Maintain and enhance reporting libraries and standards; Manage service requests and troubleshoot technical issues; Partner with Clinical Data Scientists and Data Management teams
Seniority
Senior, hands-on IC
