Establish regular lines of communication with sites and reports site progress, issues and proposed action to Clinical Operations * Performs monitoring activities related to selection, initiation, conduct (recruitment, quality data collection) and timely completion of oncology/hematology clinical trials within the assigned region. * Perform feasibility, site identification, selection and evaluation, supporting initial list of sites and recruitment targets * Ensure inspection readiness of the study and sites * Collaborates with Regional and clinical study sites to ensure timely delivery of study milestones (i.e., study startup, recruitment, database analyses, closeout, etc.) * Evaluates the quality and integrity of site practices – escalating quality and/or GCP issues with Investigators and internal team as appropriate. * BS in a relevant scientific discipline and minimum of 2 years of monitoring experience.
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