Clinical Research Coordinator II - Flowood, MS

Clinical Research Coordinator II - Flowood, MS Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. Our Site Network is a premier network of over 100 clinical research sites across the US and Europe, accelerating the path to market for novel therapies. We combine deep expertise in clinical trials with cutting‑edge AI to empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need. Responsibilities Administratively and clinically manage industry‑sponsored clinical trials including problem solving, communication, and protocol management. Lead patient recruitment activities, such as chart reviews, discussing protocols with patients, and verifying informed consent documentation to meet enrollment targets. 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. Ensure relevant study and subject‑specific information is entered into the CTMS system regularly; complete and maintain documentation study files including consent forms, source documentation, progress notes if applicable, case report forms, and investigational accountability forms, maintaining high‑quality data entry within established timelines. 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, central Iterative Health team, and PI throughout the study; resolve routine sponsor and CRO issues independently. Ensure all safety data is reviewed by the PI in a timely manner. Maintain inventory of study equipment and supplies onsite at all times. Contribute to status updates to management; implement ideas to improve site performance. Assist with routine data verification and quality control, ensuring data integrity and consistency with the prescribed study protocol. Meet requirements for data query resolution times and quality. Schedule and prepare for monitor visits. Assist 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 noncompliance. Complete and maintain case report forms per FDA guidelines, reviewing them against the patient’s medical record for completeness and accuracy. Employee Expectations Perform quality work within deadlines with or without direct supervision. Interact professionally with other employees, customers, and suppliers. Work effectively as a team contributor on all assignments. Work independently while understanding the necessity for communicating and coordinating work efforts with other employees and organizations. Qualifications Medical Assistant, LPN, Associate’s or Bachelor’s degree in a clinical or scientific‑related discipline preferred. Minimum 3 years of clinical research experience. IBD experience is a must. Ability to own issues and problem‑solve independently. Experience in phlebotomy preferred. Strong written and verbal communication skills. Ability to read, interpret, and apply clinic policies and research protocols. Ability to use standard office software. Must be able to lift up to 25 pounds. 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