The success of a clinical trial is directly dependent on the monitoring ability of the Clinical Research Associate (CRA). As an experienced CRA, I bring to the table the ability to understand complex clinical protocols and knowledge of the applicable regulations and guidelines that need to be followed. I also understand the importance of meeting stringent deadlines and effectively communicating with those involved in all facets of conducting a trial. I have experience as a study coordinator in a hospital and a CRA at both a small biotechnology start-up and at several large CROs. My long-term goal is to continue to build my skill set to be an extremely effective and efficient CRA and, ultimately, work toward a clinical research management position. Specialties: My therapeutic experience includes oncology studies (solid and liquid tumors in both adult and pediatric subjects), influenza vaccine studies, and cholesterol studies. I have experience working with Phase I - III. I have conducted all visit types, from Pre-Study through Close-Out.