Infusion Registered Nurse

requirements.</span></li> <li style="font-size: 10pt;"><span style="font-size: 10pt;">Obtain and document participant assessments while maintaining compassionate, patient-centered care.</span></li> <li style="font-size: 10pt;"><span style="font-size: 10pt;">Complete all training and documentation required during study startup for timely site activation </span></li> <li style="font-size: 10pt;"><span style="font-size: 10pt;">Foster positive participant relationships through clear communication and exceptional clinical support.</span></li> <li style="font-size: 10pt;"><span style="font-size: 10pt;">Protect the rights, safety, and welfare of all research participants in accordance with federal regulations and ethical research standards.</span></li> </ul> <ul> <li style="font-size: 10pt;"><span style="font-size: 10pt;">Complete accurate and timely source documentation, nursing notes, infusion records, case report forms, and other required study documentation.</span></li> <li style="font-size: 10pt;"><span style="font-size: 10pt;">Maintain investigational product accountability and documentation in accordance with sponsor protocols, FDA regulations, and Iterative Health policies.</span></li> <li style="font-size: 10pt;"><span style="font-size: 10pt;">Support regulatory readiness by maintaining organized study files and documentation required for sponsor monitoring visits and audits.</span></li> <li style="font-size: 10pt;"><span style="font-size: 10pt;">Ensure secure handling of Protected Health Information (PHI) and comply with HIPAA and organizational privacy policies.</span></li> </ul> <ul> <li style="font-size: 10pt;"><span style="font-size: 10pt;">Maintain adequate inventory of clinical and study supplies while supporting proper storage and handling of investigational products.</span></li> <li style="font-size: 10pt;"><span style="font-size: 10pt;">Communicate effectively with sponsors, study participants, investigators, and internal research teams throughout the study lifecycle.</span></li> <li style="font-size: 10pt;"><span style="font-size: 10pt;">Assist with study start-up, participant visits, monitoring visits, and study closeout activities as needed.</span></li> <li style="font-size: 10pt;"><span style="font-size: 10pt;">Support continuous process improvement initiatives and perform additional

responsibilities as assigned.</span></li> </ul> <ul> <li style="font-size: 10pt;"><span style="font-size: 10pt;">Perform job related duties as requested </span></li> </ul> <h4><span style="font-size: 10pt;">Required

Qualifications</span></h4> <ul> <li style="font-size: 10pt;"><span style="font-size: 10pt;">Associate or Bachelor's Nursing Degree</span></li> <li style="font-size: 10pt;"><span style="font-size: 10pt;">Active, unrestricted Registered Nurse (RN) state license </span></li> <li style="font-size: 10pt;"><span style="font-size: 10pt;">Minimum of 3 years of infusion RN experience </span></li> <li style="font-size: 10pt;"><span style="font-size: 10pt;">1–2 years of clinical research experience strongly preferred; equivalent experience in a clinical nursing environment will also be considered.</span></li> <li style="font-size: 10pt;"><span style="font-size: 10pt;">Working knowledge of Good Clinical Practice (GCP), informed consent, and human subject protection principles.</span></li> <li style="font-size: 10pt;"><span style="font-size: 10pt;">Excellent verbal and written communication skills, with the ability to educate research participants and collaborate effectively across multidisciplinary teams.</span></li> <li style="font-size: 10pt;"><span style="font-size: 10pt;">Strong organizational, time management, and critical thinking skills with the ability to prioritize multiple studies and meet competing deadlines.</span></li> <li style="font-size: 10pt;"><span style="font-size: 10pt;">Ability to read, interpret, and apply research protocols, sponsor

requirements, clinic policies, and regulatory guidelines.</span></li> <li style="font-size: 10pt;"><span style="font-size: 10pt;">Proficiency with Microsoft Office applications and the ability to quickly learn clinical research technologies, including Clinical Trial Management Systems (CTMS) and Electronic Medical Record (EMR) platforms.</span></li> <li style="font-size: 10pt;"><span style="font-size: 10pt;">Ability to work independently while contributing effectively within a collaborative, fast-paced research environment.</span></li> </ul> <h4><span style="font-size: 10pt;">Preferred

Qualifications</span></h4> <ul> <li style="font-size: 10pt;"><span style="font-size: 10pt;">Prior experience in gastroenterology (GI), hepatology, infusion services, or other specialty clinical research settings.</span></li> <li style="font-size: 10pt;"><span style="font-size: 10pt;">Experience administering investigational products, biologics, or protocol-driven infusions.</span></li> <li style="font-size: 10pt;"><span style="font-size: 10pt;">Familiarity with FDA regulations, ICH-GCP guidelines, and clinical trial documentation standards.</span></li> <li style="font-size: 10pt;"><span style="font-size: 10pt;">Experience using CTMS, Electronic Data Capture (EDC), electronic Trial Master File (eTMF), or similar clinical research systems.</span></li> <li style="font-size: 10pt;"><span style="font-size: 10pt;">ACRP or SOCRA certification (CCRC or CCRP), or a commitment to obtaining certification within the first year of employment.</span></li> </ul><div class="content-conclusion"><p><span style="font-size: 10pt;">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, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact [email protected].</span></p></div>

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