The Senior Statistical Programmer will perform data manipulation, analysis, and reporting for clinical trials using SAS while ensuring compliance with CDISC standards. They will also lead project tasks, validate datasets, and communicate effectively with cross-functional teams and clients.
The Principal Programmer CDISC SME provides subject matter expertise and leadership in the application and oversight of CDISC standards across clinical studies and regulatory submissions. They collaborate with cross-functional teams to ensure data quality, consistency, and submission readiness while mentoring staff and improving programming processes.
The Principal Statistical Programmer implements reporting and analysis activities for sponsor clinical trials while providing expert technical support to team members. They are also responsible for overseeing CRO programmers to ensure high-quality and consistent data summaries.
Lead or support Phase I-IV clinical trials by leveraging advanced SAS programming and CDISC standards. The role involves working embedded within a pharmaceutical client to deliver high-quality data manipulation and reporting.
