Sr Centralized Monitoring Analyst - (CluePoints Experience Preferred)
Core
Identify and characterize issues and trends in operational and patient clinical trial data using analytical or statistical tools to ensure operational excellence.
Role type
Senior centralized monitoring analyst (clinical trials)
Builds
Centralized monitoring plans, risk reports, findings reports, and data analytics leads
Domain
Pharmaceutical/Biotech clinical trials
Deliverable
dashboards & analysis
Required skills
Clinical trial data analysis, root cause analysis, statistical tools, regulatory guidelines compliance, SOP adherence, data confidentiality, MS Office, study documentation review, trend identification, workload prioritization
Preferred skills
CluePoints experience, data analytics lead tasks, biostatistics, clinical monitoring, data management
Technologies
CluePoints, MS Office (Word, Excel, PowerPoint), electronic study data systems
Responsibilities
Independently review and analyze clinical trial data; characterize and track evidence of issues, signals, and potential risks; perform complex and root cause analyses; contribute to centralized monitoring plan development and risk assessments; provide training and guidance to junior team members
Seniority
Senior, hands-on IC with potential lead responsibilities
