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Iterative Health is a healthcare technology and services company accelerating clinical research across gastrointestinal, hepatology, obesity, and cardiology. The company operates a network of 100+ research sites globally and combines clinical trial expertise with AI to connect sponsors with high-performing research teams.
The Clinical Research Coordinator I (RN) will support and coordinate daily clinical trial activities at a research site, playing a critical role in study conduct. This is a full-time, in-office position based in Houston, TX.
Key Responsibilities:
- Communicate study requirements to all individuals involved in the trial
- Develop and implement recruitment strategies in accordance with protocol, IRB requirements, and approvals
- Pre-screen and screen subjects for eligibility using protocol-specific inclusion/exclusion criteria
- Enter participant information and study visit procedures into the Clinical Trial Management System for accurate billing
- Maintain adequate inventory of study supplies
- Handle investigational drugs/devices according to sponsor protocol and company policy
- Complete and maintain study documentation including consent forms, source documentation, case report forms, and investigational material accountability forms
- Maintain effective communication with sponsors, research participants, site management, Regional Director, and Principal Investigator
- Manage day-to-day study activities including problem-solving, communication, and protocol management
- Collect and report ongoing patient recruitment and enrollment metrics
- Arrange secure storage of study documents per Good Clinical Practice guidelines
- Protect rights and welfare of human research participants in accordance with Federal regulations
- Cooperate with compliance and monitoring efforts regarding PHI access, use, and disclosure
- Perform other duties as assigned
Requirements:
- RN license required
- 1–3 years of clinical research coordinating experience preferred
