The CRA executes clinical monitoring activities at clinical trial sites and monitors clinical trials in accordance with ICH guidelines and GCP, local regulations, and applicable SOPs. * Performs monitoring activities related to selection, initiation, conduct (recruitment, quality data collection) and timely completion of oncology/hematology clinical trials within the assigned region. * Conducts monitoring (pre-study, initiation, routine monitoring and closeout visits per monitoring plan and applicable SOPs * Conducts co-monitoring visits, if required * Completes monitoring visit reports in accordance with ICH-GCP, BeOne Medicines standards and SOP * Establish regular lines of communication with sites and reports site progress, issues and proposed action to Clinical Operations * Collaborates with Regional and clinical study sites to ensure timely delivery of study milestones ...
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