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Iterative Health in Clifton, NJ, seeks a Clinical Research Coordinator II to run industry-sponsored trials from start-up to closeout with minimal supervision, covering patient recruitment, consent talks, protocol visits, vitals, and data entry. CTMS/EDC proficiency and careful record keeping are essential.
The role requires 3–5 years in clinical research or healthcare, strong organizational skills, and the ability to read and apply protocols.
This is a hands-on research coordinator role where one person runs industry-sponsored trials from start-up to closeout with little supervision. It covers patient recruitment, consent talks, protocol visits, clinical tasks like vitals, ECGs and blood draws, lab shipping, and accurate records and data entry. A strong candidate has 3 to 5 years in clinical research or healthcare, is organized and careful with detail, and can read a protocol and apply it correctly. Experience in stomach, liver or heart research and a coordinator certification would help.
AI can speed up the paperwork side of trials, such as finding likely patients in charts, tracking enrollment and spotting data gaps. The company says it pairs AI with its research network, so a coordinator may use these tools to work faster. What stays human is talking with patients, explaining a study and earning trust. Careful judgment on safety, protocol rules and accurate source records also stays with the person.
Working here would likely mean using the company's technology for finding patients, tracking studies and managing data in community care sites. That is practical exposure to how AI supports trial recruitment and operations. To build this experience, get comfortable with CTMS and EDC systems, learn how chart review and enrollment tracking can be made more efficient, and practice checking AI-assisted outputs against source records.
This is our own read, written from the employer's posting and the company's Spotlight. The employer's posting is the source of truth for the role.
Iterative Health embeds clinical research into community care settings, and per the company, runs trials 2x faster to activate sites and 3x higher patient enrollment.