<div class="content-intro"><p><span style="font-size: 10pt;">Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes.</span></p> <p><span style="font-size: 10pt;">We built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology. By combining deep clinical trial expertise with cutting-edge AI, we connect sponsors' scientific ambitions with high-performing research teams that expedite and expand access to novel therapeutics for patients in need. Today, Iterative Health is headquartered in Cambridge, Massachusetts, and New York City with 250+ employees world-wide.</span></p> <p> </p></div><p><span style="font-size: 10pt;">A Clinical Research Coordinator I – RN at Iterative Health is an essential member of the site research team, supporting, facilitating, and coordinating the daily execution of clinical trials across our network. This role is at the heart of every study — managing patient interactions, ensuring protocol compliance, maintaining data integrity, and keeping the operational machinery of clinical research running smoothly. </span></p> <p><span style="font-size: 10pt;">The ideal candidate brings clinical research experience, a patient-first mindset, strong attention to detail, and the ability to thrive in a fast-paced, protocol-driven environment. This role provides a strong foundation for success while offering a clear path for professional growth within Iterative Health's expanding site network. </span></p> <h2><span style="font-size: 10pt;"><strong>Where You’ll Drive Impact</strong></span></h2> <ul> <li style="font-size: 10pt;"><span style="font-size: 10pt;">Administratively and clinically manage industry-sponsored clinical trials, including problem-solving, communication, and protocol management.</span></li> <li style="font-size: 10pt;"><span style="font-size: 10pt;">Schedule all patient research visits and procedures in accordance with protocol requirements.</span></li> <li style="font-size: 10pt;"><span style="font-size: 10pt;">Ensure relevant study and subject-specific information is entered into the CTMS on a regular basis.</span></li> <li style="font-size: 10pt;"><span style="font-size: 10pt;">Complete and maintain study documentation including consent forms, source documentation, progress notes, case report forms, and investigational accountability forms.</span></li> <li style="font-size: 10pt;"><span style="font-size: 10pt;">Complete and maintain case report forms per FDA guidelines, reviewing them against patient medical records for completeness and accuracy.</span></li> <li style="font-size: 10pt;"><span style="font-size: 10pt;">Schedule and prepare for monitor visits.</span></li> <li style="font-size: 10pt;"><span style="font-size: 10pt;">Maintain inventory of study equipment and supplies onsite at all times.</span></li> </ul> <ul> <li style="font-size: 10pt;"><span style="font-size: 10pt;">Lead patient recruitment activities including chart reviews, protocol discussions with patients, and verification of informed consent documentation.</span></li> <li style="font-size: 10pt;"><span style="font-size: 10pt;">Conduct patient visits as outlined within each study protocol.</span></li> <li style="font-size: 10pt;"><span style="font-size: 10pt;">Act as the primary point of contact for study participants throughout the course of the study.</span></li> </ul> <ul> <li style="font-size: 10pt;"><span style="font-size: 10pt;">Dispense study medication, collect vital signs, and perform ECGs per protocol.</span></li> <li style="font-size: 10pt;"><span style="font-size: 10pt;">Perform blood draws; process and ship specimens per study protocol and IATA regulations.</span></li> <li style="font-size: 10pt;"><span style="font-size: 10pt;">As assigned: place IVs, administer IV medications and fluids, give intramuscular and subcutaneous injections, monitor patients during infusion, and discharge patients in accordance with protocol and site policies.</span></li> </ul> <ul> <li style="font-size: 10pt;"><span style="font-size: 10pt;">Adhere to Research SOPs, Good Clinical Practice (GCP) guidelines, and study protocols at all times.</span></li> <li style="font-size: 10pt;"><span style="font-size: 10pt;">Assist with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocols.</span></li> <li style="font-size: 10pt;"><span style="font-size: 10pt;">Ensure all safety data is reviewed by the PI in a timely manner.</span></li> <li style="font-size: 10pt;"><span style="font-size: 10pt;">Cooperate with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI; report instances of noncompliance to the appropriate compliance office.</span></li> <li style="font-size: 10pt;"><span style="font-size: 10pt;">Assist the study team in protecting the rights and welfare of all human research participants in accordance with federal regulations.</span></li> <li style="font-size: 10pt;"><span style="font-size: 10pt;">Maintain ongoing communication with the CRO, sponsor, research participants, Site Manager, and PI throughout th