With over two years of clinical research experience, I am a highly detail-oriented Clinical Research Coordinator. From developing protocols and adhering to regulatory requirements to following protocol guidelines and ethical standards, I am skilled in all aspects of clinical research. My main competencies include patient recruitment, informed consent procedures, data collection, and monitoring of adverse events. I conduct research in compliance with Good Clinical Practice (GCP) standards. I am passionate about providing an opportunity to further medical expertise through quality research.