Clinical Research Coordinator I - Nurse

Clinical Research Coordinator I - Nurse - Cordova, TN Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. Our Site Network comprises over 70 global clinical research sites focused on gastrointestinal and hepatology therapies. We drive the success of partner sites by providing tech‑enabled services and cutting‑edge AI expertise. We are seeking a full‑time, experienced Clinical Research Coordinator (CRC) to support, facilitate, and coordinate daily clinical trial activities at Cordova, TN. Responsibilities Administratively and clinically manage industry‑sponsored clinical trials, including problem solving, communication, and protocol management. Lead patient recruitment activities, e.g., perform chart reviews, discuss protocols with patients, and verify informed consent documentation. Schedule all patient research visits and procedures in accordance with protocol requirements. Conduct patient visits as outlined within each study protocol. Dispense study medication, collect vital signs, and perform ECGs. Perform blood draws, process and ship specimens per study protocol and IATA regulations. Administer IV medication, place IVs, and manage IV tubing and infusions; give intramuscular and subcutaneous injections per protocol. Ensure relevant study and subject‑specific information is entered into the CTMS system on a regular basis; maintain documentation study files including consent forms, source documentation, progress notes, case report forms, and investigational accountability forms. Act as point of contact for study participants. Adhere to Research SOPs, Good Clinical Practices, and the study protocols. Maintain ongoing communication with the CRO, sponsor, research participants, Site Manager, and PI throughout the study. Ensure all safety data is reviewed by the PI in a timely manner. Maintain inventory of study equipment and supplies onsite at all times. Assist in communication of status and results to management. Assist the study team in data verification and quality control, ensuring data integrity and consistency with the prescribed protocol. Schedule and prepare for monitor visits. Assist the study team in protecting the rights and welfare of all human research participants in accordance with federal regulations. Cooperate with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI and report instances of non‑compliance. Complete and maintain case report forms per FDA guidelines, reviewing them against the patient’s medical record for completeness and accuracy. All employees are expected to perform quality work within deadlines, interact professionally, work effectively as a team contributor, and coordinate work efforts with other employees and organizations. As set forth in Iterative Health’s Equal Employment Opportunity policy, we do not discriminate on the basis of any protected group status under any applicable law. #J-18808-Ljbffr Iterative Health