Centralized Monitoring Analyst (Level I & II)
Core
Review clinical trial data to identify, characterize, and track operational issues, signals, and potential risks using analytical tools to ensure data quality and support project teams.
Role type
Centralized Monitoring Analyst (Level I & II)
Builds
Clinical trial data quality reports and risk characterizations for pharmaceutical and biotech clients
Domain
Life Sciences / Clinical Trials / Data Analytics
Deliverable
dashboards & analysis
Required skills
Clinical trial monitoring, data analysis, statistical tools, regulatory guidelines (SOPs), MS Office, medical terminology, risk characterization
Preferred skills
Biostatistics, data management, prior clinical monitoring experience
Technologies
Electronic study data systems, department databases, MS Office (Word, Excel, PowerPoint)
Responsibilities
Review clinical trial data per centralized monitoring plan, characterize and track evidence of issues and risks, document review results, support review set-up and reporting
Seniority
Mid-level, individual contributor