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.
Role type
Centralized Monitoring Analyst (Level I & II)
Builds
Risk characterization reports and findings for clinical trial projects
Domain
Clinical trials / Pharmaceutical industry
Deliverable
dashboards & analysis
Required skills
Data analysis, statistical tools, regulatory guidelines knowledge, SOP adherence, attention to detail, data confidentiality, computer skills (MS Office), study documentation interpretation, medical terminology understanding
Preferred skills
Clinical monitoring experience, data management, biostatistics
Technologies
MS Office (Word, Excel, PowerPoint), electronic study data systems
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 database updates
Seniority
Entry to Mid-level, individual contributor