As a clinical research assistant with 1.5 years’ experience working to coordinate Radiation Oncology clinical trials on site for external sponsors, I am actively involved in supporting clinical trials by conducting essential tasks such as site feasibility, set-up consisting of site initiation visits, study files and documentation, training as well as study visits, data management and supervising monitoring visits. While coordinating a trial site I am adept at leading project management and conducting all trials within Good Clinical Practice (GCP), while communicating with external sponsors in regard to the performance of trials, from enrolment to close-out.