Principal Clinical Programmer (DM SAS) - Serbia, hybrid

Tasks

• Assist with sponsor audits
• Attend Quick Start Camps
• Conduct senior review for study deliveries
• Configure coding and edit checks
• Coordinate clinical programming activities
• Create database setups
• Develop clinical programming software
• Execute user acceptance testing
• Generate listings and custom reports
• Lead clinical programming for concurrent studies
• Lead development activities
• Lead training and guidance for programming teams
• Maintain annotated case report forms
• Manage change orders
• Manage project resources
• Monitor application workflow alerts and system errors
• Monitor scope and budgets
• Perform application updates and integration
• Provide application administration and technical support
• Provide second tier help desk support
• Provide technology support for clinical programming teams
• Review and finalize specifications
• Serve as subject matter expert for Oracle Inform
• Support import and export processing
• Validate SAS programs

Perks/Benefits

• N/A

Skills/Tech-stack

Acceptance Testing | Change Management | Clinical data | Clinical data management | Clinical programming | Data Management | Medidata | Oracle Inform | Oracle OC | Oracle RDC | Rave | SAS | SAS Validation | SQL | User Acceptance | User Acceptance Testing