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Clinical Research Coordinator Position Details Shift: Monday to Friday, 7:00 AM - 4:00 PM (adjustable) Location: Port Charlotte, FL 33952 Position Type: Contract Health Requirements Hepatitis B Vaccine Influenza Vaccine (seasonal or signed declination required) MMR Titers Varicella Titers Position SummaryThe Clinical Research Coordinator is responsible for managing multiple research protocols and acting as a key liaison between local investigators, industry sponsors, and other stakeholders. Under direct supervision, the coordinator will develop a foundational understanding of research operations and human subject research regulations. Major Responsibilities Adhere to the organization's "Code of Conduct" philosophy and "Mission and Value Statement." Complete all assigned training requirements by their due dates. Conduct routine operational tasks for multiple research protocols. Serve as a liaison between site research personnel, industry sponsors, and supervisors. Collaborate with site departments, including finance, hospital administration, and the local IRB when applicable. Coordinate assessment schedules from feasibility submission to study closeout. Review study design and inclusion/exclusion criteria with physicians and patients. Ensure patient protection by verifying informed consent procedures and protocol compliance. Maintain data integrity through careful source document review and monitoring for missing or implausible data. Develop study-specific source documentation tools when not provided by the sponsor. Collect, complete, and enter data into case report forms or electronic data capture systems. Manage drug, device, and supply shipments as required. Ensure timely and accurate data submission. Track and report adverse events, serious adverse events, protocol waivers, deviations, and violations. Education & Experience Required: Bachelor's Degree or equivalent combination of education and experience. Preferred: Degree in a related field. Required: Minimum of 1 year of relevant experience or equivalent combination of education and experience. Licenses, Certifications, & Training Preferred: Certified Clinical Research Coordinator.Knowledge Familiarity with organizational policies, standard operating procedures, and systems. Basic understanding of ICH guidelines and the Code of Federal Regulations in clinical research. Basic knowledge of medical terminology.Skills Effective communication. Strong organizational and time management skills. Proficiency in basic clinical trial procedures, including ECG acquisition, phlebotomy, and specimen handling, processing, storage, and shipping.Abilities Strong interpersonal skills. Self-motivated with a meticulous eye for detail.Clinical CompetenciesThis role may require proficiency in clinical tasks such as ECG, phlebotomy, and specimen handling (centrifuging, storing, and shipping). Core competencies will be evaluated annually, with training and/or certification provided as required by protocol. Travel Requirements Occasional Travel: The role may require travel from time to time, but not on a regular basis.