About the role
Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. 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. At Iterative Health, we're transforming clinical research by making trials more accessible, efficient, and patient-centered. As a Infusion Registered Nurse, you'll play a role in delivering safe, protocol-driven clinical care while supporting the successful execution of research studies. Working closely with Principal Investigators, Clinical Research Coordinators, and site leadership, you'll ensure study participants receive high-quality care while maintaining the integrity of clinical trial data and regulatory compliance. Where You’ll Drive Impact Administer investigational products, infusions, injections, and other protocol-required treatments in accordance with study protocols, physician orders, and Good Clinical Practice (GCP). Perform protocol-specific clinical procedures including vital signs, specimen collection, ECGs, medication administration, and participant assessments. Monitor participants before, during, and after study procedures, identifying aComplete all training and documentation required during study startup for timely site activation nd responding appropriately to adverse events or changes in clinical status. Collaborate with Principal Investigators, Clinical Research Coordinators, and study teams to ensure protocol compliance and participant safety. Educate research participants on study procedures, treatment expectations, and follow-up
requirements. Obtain and document participant assessments while maintaining compassionate, patient-centered care. Complete all training and documentation required during study startup for timely site activation Foster positive participant relationships through clear communication and exceptional clinical support. Protect the rights, safety, and welfare of all research participants in accordance with federal regulations and ethical research standards. Complete accurate and timely source documentation, nursing notes, infusion records, case report forms, and other required study documentation. Maintain investigational product accountability and documentation in accordance with sponsor protocols, FDA regulations, and Iterative Health policies. Support regulatory readiness by maintaining organized study files and documentation required for sponsor monitoring visits and audits. Ensure secure handling of Protected Health Information (PHI) and comply with HIPAA and organizational privacy policies. Maintain adequate inventory of clinical and study supplies while supporting proper storage and handling of investigational products. Communicate effectively with sponsors, study participants, investigators, and internal research teams throughout the study lifecycle. Assist with study start-up, participant visits, monitoring visits, and study closeout activities as needed. Support continuous process improvement initiatives and perform additional
