Clinical Research Coordinator I - Nurse

Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 70+ clinical research sites across US and Europe accelerating the path to market for gastrointestinal (GI) and hepatology novel therapies. Our focus is on driving the success and growth of our partner sites by empowering them with tech-enabled services. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need. Clinical Research Coordinator I - Nurse We are seeking a full-time, experienced Clinical Research Coordinator (CRC). The CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study. Responsibilities Administratively and clinically manage industry-sponsored clinical trials including problem solving, communication and protocol management. Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation. Schedule all patient research visits and procedures consistent 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. If assigned, place IVs, administer IV medication, and fluids according to protocol. Monitor patients’ IV medications and tubing. Give intramuscular and subcutaneous injections according to protocol. Monitor patients during infusion and discharge patients as policies indicate. Enter relevant study and subject specific information into the CTMS system on a regular basis; complete and maintain documentation study files including, but not limited to, consent forms, source documentation, progress notes (if applicable), 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 course of 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. Participate actively in communication of status and results to management. Assist with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocol. Schedule and prepare for monitor visits. Assist the Study Team in protection of the rights and welfare of all human research participants involved in research 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, and review them against the patient’s medical record for completeness and accuracy. Iterative Health 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. At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, the hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact View email address on click.appcast.io. #J-18808-Ljbffr