Houston, Texas, 77002

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Full Time
Onsite
Clinical Research Coordinator I – Houston, TX

The Clinical Research Coordinator supports and facilitates daily clinical trial activities, including patient recruitment, screening, and protocol management. They are responsible for maintaining study documentation, ensuring regulatory compliance, and communicating effectively with sponsors and research teams. Candidates must hold a valid RN license to be considered for this role. A minimum of 1-3 years of clinical research coordinating experience is preferred.


Iterative Health provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
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Clinical Research Coordinator I – Houston, TX
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supports..pdf, .doc, .docx, or .txt file