Senior Clinical Research Associate with eight years of experience. Fluent in monitoring Enterics, Vaccine Development, Oncology, Neurology, Ophthalmology, and Nephrology phase I - III trials single or multi-site trials throughout the United States and Canada. Experienced in developing documents for trial start-up, maintaining central regulatory documents including the Clinical Monitoring Plan, Protocol, SOPs, and safety plans, and knowledgeable about conducting Site Qualification Visits through Close-Out Visits and Audit preparation. Excels at time management, communications between site, internal, and Sponsor/external staff, creating trackers to ensure all expectations of monitoring and trial execution are effectively completed, and action item resolution.Highly detail and goal-oriented with all deliverables and monitoring requirements. Able to identify unique topics to train and assist CRAs on a plethora of study-related topics.