​​Senior Associate, Central Monitor, Data Surveillance, Clinical Data Sciences​

Tasks

• Define Key Risk Indicators
• Ensure clinical trial data quality
• Follow up issue resolution
• Maintain quality control documentation for monitoring
• Provide program oversight
• Provide technical support for database issues
• Review system outputs for signal and action management
• Set up and test risk based monitoring system
• Support signal and action mitigation

Perks/Benefits

• Hybrid work

Skills/Tech-stack

Action Management | CRF design | Clinical data | Clinical data management | Clinical trial | Clinical trial database | DMP | Data Management | Data Quality | Data cleaning | Database Design | Database Programming | Edit checks | ICH GCP | Java | Key Risk Indicators | Microsoft Excel | Microsoft PowerPoint | Microsoft Project | Microsoft Word | Oracle | PL/SQL | Relational Database | Relational Database Design | Risk indicators | Risk-Based Monitoring | Risk-based | S&OP | SAS | Signal Action Management | Windows