Associate Central Monitor, Data Surveillance, Clinical Data Sciences
ARG - San Isidro, Argentina
USD 79K-131K (estimate) Mid-level Full Time
Tasks
- Align analytics system with ICH GCP and SOPs
- Define Key Risk Indicators
- Develop risk based monitoring analytics system
- Maintain quality control documentation
- Review system outputs and signals
- Set up and test study level monitoring systems
- Support central monitoring activities
- Support signal and action management
- Support study risk based monitoring compliance
Perks/Benefits
Skills/Tech-stack
Clinical trial | Clinical trial protocols | Data cleaning | Database Design | Edit checks | ICH GCP | Java | Key Risk Indicators | Operating procedures | Oracle | PLSQL | Python | R | Relational Database | Relational Database Design | Risk indicators | Risk-Based Monitoring | Risk-based | SAS | SQL | Standard Operating Procedures | Trial Protocols
Education
Bachelor of Engineering | Bachelor of Science | Master of Science | PhD
Roles
Regions
Countries
States
Cities
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