Clinical Research Coordinator I: Patient‑Focused Trials

Iterative Health; Webster (TX); On-site; USD 52,000 - 72,000; Full time

Job summary

Iterative Health is seeking a Clinical Research Coordinator I to support the day‑to‑day execution of clinical trials at our Webster, TX site. You will coordinate patient visits, assist with documentation, and ensure protocol compliance, patient safety, and data integrity.

The role requires a scientific/healthcare degree and 1–3 years of experience. You will collaborate with sponsors, CROs, investigators, and internal teams to advance innovative therapies while maintaining rigorous study

Qualifications

• Associate’s or Bachelor’s degree in a scientific, healthcare, or related discipline required.
• 1–3 years of clinical research or healthcare experience required.
• Must be able to perform blood draw, medical review (blood pressure, height, weight etc.) & EKGs, as applicable by state law.

Responsibilities

• Coordinate patient visits, procedures, and study activities according to protocol.
• Maintain accurate study documentation and CTMS updates.
• Support patient recruitment and retention activities and informed consent coordination.
• Ensure compliance with GCP, HIPAA, and site SOPs.

Skills

Blood draw

EKGs

Protocol review

Data entry

Attention to detail

Education

Associate’s or Bachelor’s degree

Tools

CTMS

EDC systems

Office software

Job description

Iterative Health is seeking a Clinical Research Coordinator I to support the day‑to‑day execution of clinical trials at our Webster, TX site. You will coordinate patient visits, assist with documentation, and ensure protocol compliance, patient safety, and data integrity.

The role requires a scientific/healthcare degree and 1–3 years of experience. You will collaborate with sponsors, CROs, investigators, and internal teams to advance innovative therapies while maintaining rigorous study