Clinical Research Coordinator
CurrentAccomplished Clinical Research Coordinator with 3 years of experience in planning, organizing, and overseeing clinical trials.Demonstrated proficiency in regulatory compliance, ensuring adherence to ethical standards and guidelines.Proven track record of successfully coordinating multi-site trials, managing diverse stakeholders, and meeting project timelines.Expertise in participant informed consent processes, contributing to successful trial enrollment.Comprehensive knowledge of Good Clinical Practice (GCP) and FDA regulations, ensuring the highest standards of research integrity.Collaborative team player, fostering effective communication among cross-functional teams, investigators, and sponsors.Proficient in data collection, entry, and management using electronic data capture (EDC) systems.Strong organizational skills with a keen attention to detail, ensuring accurate and timely documentation.Successful preparation for site initiation and monitoring visitsContinuous commitment to professional development through ongoing education and staying current with industry trends.Dedicated to enhancing the quality of clinical research through a patient-centric approach and ethical conduct