Sort clinical trial responsibilities
Classify common trial responsibilities to the role that is primarily accountable.
Sort each task to the role that is primarily accountable for it. Investigator or site Sponsor or CRO IRB or ethics committee Coordinator delegated task Assess participant medical care and safety decisions during the trial Make protocol eligibility judgment involving medical interpretation Design sponsor oversight and quality management for the trial Set and execute the monitoring plan through sponsor oversight Review and approve the protocol and consent materials before conduct Review continuing participant-protection information as required Call participant with visit reminder and fasting instructions per delegation Enter source-supported visit data into EDC after review checks File approved documents in the…
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