Infusion Registered Nurse

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.

Responsibilities

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 and 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 responsibilities as assigned.; Perform job related duties as requested.

Requirements

Associate or Bachelor's Nursing Degree; Active, unrestricted Registered Nurse (RN) state license; Minimum of 3 years of infusion RN experience; 1–2 years of clinical research experience strongly preferred; equivalent experience in a clinical nursing environment will also be considered.; Working knowledge of Good Clinical Practice (GCP), informed consent, and human subject protection principles.; Excellent verbal and written communication skills, with the ability to educate research participants and collaborate effectively across multidisciplinary teams.; Strong organizational, time management, and critical thinking skills with the ability to prioritize multiple studies and meet competing deadlines.; Ability to read, interpret, and apply research protocols, sponsor requirements, clinic policies, and regulatory guidelines.; 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.; Ability to work independently while contributing effectively within a collaborative, fast-paced research environment.

Nice to have

Prior experience in gastroenterology (GI), hepatology, infusion services, or other specialty clinical research settings.; Experience administering investigational products, biologics, or protocol-driven infusions.; Familiarity with FDA regulations, ICH-GCP guidelines, and clinical trial documentation standards.; Experience using CTMS, Electronic Data Capture (EDC), electronic Trial Master File (eTMF), or similar clinical research systems.; ACRP or SOCRA certification (CCRC or CCRP), or a commitment to obtaining certification within the first year of employment.