Clinical Research Coordinator

We are seeking a highly skilled and experienced Clinical Research Coordinator to join an expanding research team in San Antonio, Texas. 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 Responsibilities Lead and oversee the coordination of multiple clinical trials in compliance with FDA regulations, ICH-GCP guidelines, and institutional policies Serve as the primary point of contact for sponsors, monitors, and regulatory bodies Obtain and document informed consent from study participants in accordance with ethical and regulatory standards Perform and oversee clinical procedures, including phlebotomy, vital signs, ECGs, and specimen handling per study protocols Review, interpret, and manage laboratory results, ECGs, and other clinical data, ensuring timely investigator review and follow-up Identify, document, and report Adverse Events (AEs) and Serious Adverse Events (SAEs) promptly to the Principal Investigator and sponsor Coordinate and manage patient scheduling, ensuring visits occur within protocol-specified windows Dispense investigational products per protocol, provide medication education, and monitor subject compliance and progress Requirements: 5+ years of experience as a Clinical Research Coordinator in a clinical research setting Strong background in industry sponsored trials and working knowledge of ICH-GCP guidelines Phlebotomy certification and clinical skills (vital signs, ECGs, specimen processing) .Exceptional organizational skills, attention to detail, and ability to manage multiple studies simultaneously Strong communication and leadership abilities with a collaborative approach to teamwork #J-18808-Ljbffr