Clinical Trial Management System (CTMS), Serious Adverse Event (SAE) Reporting, Microsoft Office, Clinical Trial Process, Phase I Monitoring, Fortrea SOPs, Source Document Verification, eTMF, Investigational Product Inventory and Accountability, eCRF Review, Clinical Research Terminology, clinical monitoring, Site Management, ICH GCP Guidelines, Regulatory Requirements, Source Document Review, Query Generation and Resolution, Data Management Systems

Data Analytics, Onsite monitoring, ICH Guidelines, Electronic Data Capture, Source Document Review, Risk-based monitoring, Clinical data integrity