Dedicated and highly skilled Clinical Research Coordinator with three years of comprehensive experience in the successful management and oversight of clinical trials. Proficient in utilizing Microsoft Office applications and data entry systems such as Medrio and Medidata, ensuring accurate and efficient record-keeping. Adept at fostering effective communication among team members and participants, with strong collaborative and strategic planning abilities. In-depth knowledge of medical terminology, coupled with a meticulous adherence to Institutional Review Board (IRB) regulations. Demonstrated expertise in critical thinking, issue resolution, and data analysis to enhance study outcomes. Proven track record of overseeing day-to-day operations, ensuring tasks are completed with precision and efficiency. Seeking to contribute my skills and experience to a dynamic research team in a challenging and rewarding environment.