At EthiTrials CRO, I maintained Trial Master Files, checked document completeness, and supported REB/IEC submissions. I also conducted source data verification and monitored protocol compliance.
As a Clinical Research Consultant at EthiTrials CRO, I supported remote site activities through document management and communications, handled system queries, and assisted with study closeout and document reconciliation. On a digital stethoscope study, I led participant recruitment, protocol compliance, and feedback documentation.
