Clinical Research Coordinator III | FKP - Port Charlotte

Clinical Research Coordinator III Florida Kidney Physicians (FKP) | Port Charlotte, FL Powered by Panoramic Science Location:2852 Tamiami Trail, Suite 1Port Charlotte, FL 33952 Advance the Future of Kidney Care Through Clinical Research Are you an experienced Clinical Research Coordinator looking to take ownership of a thriving research program while making a meaningful impact on patient lives? Florida Kidney Physicians (FKP), one of Florida's leading nephrology practices, is seeking a highly motivated Clinical Research Coordinator III to lead clinical trial operations at our Port Charlotte research site. This is an exciting opportunity to work alongside renowned nephrologists and research professionals while helping bring innovative therapies to patients with chronic kidney disease and related conditions. As part of the Panoramic Science research network, you'll have access to industry-leading resources, cutting-edge clinical trials, and opportunities to contribute to groundbreaking advancements in nephrology, cardiovascular, metabolic, and rare disease research. Why Join FKP and Panoramic Science? Lead and manage clinical research studies at a dedicated research site Work directly with Principal Investigators and patients Participate in innovative nephrology and chronic disease research Join one of the nation's largest kidney-focused research networks Collaborate with experienced research professionals across the country Make a direct impact on patient care and treatment innovation Position Summary The Clinical Research Coordinator III serves as the site-level leader for clinical research operations, ensuring successful study execution, patient recruitment, enrollment, retention, and data quality while maintaining compliance with protocol requirements, Good Clinical Practice (GCP), FDA regulations, and site standard operating procedures. This role requires a highly organized, proactive professional who can independently manage multiple studies, mentor research staff, and drive enrollment performance while maintaining exceptional patient care and regulatory compliance. Key Responsibilities Study Start-Up & Site Management Review and understand assigned research protocols Assess site readiness and study resource requirements Train clinic staff on study objectives and eligibility criteria Implement workflows to optimize study recruitment and execution Coordinate study activation activities with internal and external stakeholders Patient Recruitment & Enrollment Identify and pre-screen potential research participants Collaborate with providers and clinic staff to increase patient referrals Conduct informed consent discussions and documentation Partner with central research teams to meet enrollment goals Maintain strong patient engagement and retention throughout study participation Clinical Trial Execution Conduct protocol-required patient visits and assessments Perform vital signs, height, weight, ECGs, specimen collection, and other study procedures Administer questionnaires and study-related materials Dispense and collect investigational products Process laboratory specimens according to protocol requirements Maintain accurate source documentation and study records Data & Regulatory Compliance Complete timely and accurate data entry following ALCOA principles Maintain regulatory compliance with GCP, FDA, IRB, and sponsor requirements Report adverse events and serious adverse events within required timelines Prepare for sponsor and monitoring visits Maintain investigational product accountability and temperature logs Resolve data queries and monitoring findings promptly Leadership & Mentorship Coach and mentor Research Coordinators and site staff Assist with process improvement initiatives Support study planning, prioritization, and milestone management Foster a culture of quality, compliance, and patient safety Qualifications Required Minimum 5-7 years of clinical research experience Strong understanding of GCP, FDA regulati…