Detail-oriented Clinical Trial Coordinator with a Master’s in Health Informatics and experience in healthcare data management, regulatory compliance, and patient monitoring. Strong background in data collection, protocol adherence, and trial coordination in healthcare settings. Skilled in working with IRB regulations, patient recruitment, electronic data capture (EDC) systems, and clinical research methodologies. Adept at collaborating with cross-functional teams, including investigators, sponsors, and regulatory bodies, to ensure efficient and compliant execution of clinical trials. Dedicated clinical research coordinator experienced in complying with study protocols, standard operating procedures and good clinical practices. Practiced problem-solver with strong attention to detail. Prepared to offer several years' experience in the field and take on a fast-paced position.