Clinical Research Coordinator

We are seeking an experienced Clinical Research Coordinator to join an expanding research team in Miami, FL. The ideal candidate will bring advanced expertise in clinical trial coordination, regulatory compliance, and patient management, as well as leadership in supporting junior staff and contributing to study planning and execution.Key ResponsibilitiesOversee the coordination of multiple clinical trials in compliance with FDA regulations, ICH-GCP guidelines, and institutional policiesObtain and document informed consent from study participants in accordance with ethical and regulatory standardsPerform clinical procedures, including phlebotomy, vital signs, ECGs, and specimen handling per study protocolsReview, interpret, and manage laboratory results, ECGs, and other clinical data, ensuring timely investigator review and follow-upIdentify, document, and report Adverse Events (AEs) and Serious Adverse Events (SAEs) promptly to the Principal Investigator and sponsorCoordinate and manage patient scheduling, ensuring visits occur within protocol-specified windowsDispense investigational products per protocol, provide medication education, and monitor subject compliance and progressRequirements:3+ years of experience as a Clinical Research Coordinator in a clinical research settingStrong background in industry sponsored trials and working knowledge of ICH-GCP guidelinesPhlebotomy certification and clinical skills (vital signs, ECGs, specimen processing)Exceptional organizational skills, attention to detail, and ability to manage multiple studies simultaneouslyStrong communication and leadership abilities with a collaborative approach to teamworkIf you are an experienced clinical research professional passionate about advancing medical knowledge and improving patient care, we invite you to apply. Join our Miami-based research team and contribute to innovative, life-changing clinical studies that make a real impact.