Clinical Research Coordinator I - Nurse

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 worldwide. The Iterative Health Site Network is a premier network of 80+ global clinical research sites 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. We are seeking a full‑time, experienced Clinical Research Coordinator – Nurse. The CRC‑RN supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.

Responsibilities

• Communicate study requirements to all individuals involved in the study.
• Develop and implement recruitment strategies in accordance with GI Alliance RESEARCH and IRB requirements and approvals.
• Pre‑screen and screen subjects for eligibility using protocol‑specific inclusion and exclusion criteria.
• Enter participant information and study visit procedures into the Clinical Trial Management System to ensure billing to appropriate funding sources.
• Maintain adequate inventory of study supplies.
• When handling investigational drugs/devices, follow the sponsor protocol and/or GI Alliance RESEARCH Policy on Investigational Drug/Device Accountability.
• Complete study documentation and maintenance of study files in accordance with sponsor requirements and GI Alliance RESEARCH policies and procedures including, but not limited to, consent forms, source documentation, narrative notes if applicable, case report forms, and investigational material accountability forms.
• Maintain effective and ongoing communication with sponsor, research participants, site manager, Regional Director, and PI during the course of the study.
• Manage the day‑to‑day activities of the study including problem solving, communication and protocol management.
• Collect and report ongoing patient recruitment/enrollment metrics to site manager and PI.
• Arrange secure storage of study documents that will be maintained according to Good Clinical Practice guidelines or for the contracted length of time, whichever is longer.
• Protect the rights and welfare of all human research participants involved in research in accordance with Federal regulations.
• Cooperate with GI Alliance RESEARCH compliance and monitoring efforts regarding the access, use, and disclosure of PHI and report instances of noncompliance to the appropriate compliance office.
• Perform other duties as assigned.

Qualifications

• RN license required.
• 1‑3 years of Clinical Research Coordinating experience preferred.