Clinical Research Associate with extensive monitoring experience along with entry level and lead CRA work experience. Worked with site staff to schedule, plan and conduct study visits (pre-study, initiation, interim monitor, and close-out) in accordance with ICH/GCPs, SOPs, and the study protocol. Trained site staff as well as new monitors and in-house CRAs on all aspects of the role including: protocol training, EDC entry/query resolution, and investigational product accountability. Worked in a team environment for a common goal of study completion and potential study drug approval.