Associate Central Monitor, Data Surveillance, Clinical Data Sciences
USD 78K-127K (estimate) Mid-level Full Time
Tasks
- Assist implementation of quality processes
- Define key risk indicators in study system
- Ensure RBM analytics align with protocol ICH GCP and SOPs
- Maintain RBM quality control documentation
- Review system outputs and manage signals and actions
- Set up and test study level risk based monitoring analytics
- Support central monitoring activities to ensure data completeness and accuracy
Perks/Benefits
Skills/Tech-stack
CRF design | Clinical data | Clinical data management | Clinical trial | Clinical trial database | Clinical trial protocol | DMPs | Data Management | Data Quality | Data cleaning | Data quality control | Database Design | Database Programming | Edit Check | Edit Check Specifications | ICH GCP | Java | Key Risk Indicators | Microsoft Excel | Microsoft PowerPoint | Microsoft Project | Microsoft Word | Oracle | PL/SQL | Python | Quality Control | R | Relational Database | Relational Database Design | Risk indicators | Risk-Based Monitoring | Risk-based | SAS | SQL | Windows
Education
Bachelor of Engineering | Bachelor of Science | Master of Science | PhD
Regions
Countries
States
Cities
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