Clinical Research Coordinator I — Drive Patient-Centric Trials

Iterative Health; Iowa (LA); On-site; USD 42,000 - 62,000; Full time

Job summary

Iterative Health is seeking a Clinical Research Coordinator I to support day-to-day trial activities, ensure protocol compliance, and safeguard patient safety across GI, hepatology, obesity, and cardiology studies. You will work with sponsors, CROs, investigators, and internal teams to deliver high-quality clinical research and patient experiences.

Responsibilities include coordinating visits, procedures, data entry, maintaining study documents, assisting with recruitment, and ensuring

Qualifications

• Associate’s or Bachelor’s degree in a scientific, healthcare, or related discipline is required.
• 1–3 years of clinical research or healthcare experience is required.
• Ability to perform essential procedures (blood pressure, vitals, ECGs) as permitted by state law.

Responsibilities

• Coordinate patient visits, procedures, and study activities according to protocol timelines.
• Maintain accurate study documentation and regulatory compliance across site SOPs and GCP.
• Support patient recruitment, informed consent, and data entry with high data quality.

Skills

Organizational skills

Attention to detail

Prioritization

Communication

Protocol interpretation

Education

Associate or Bachelor degree

Tools

CTMS

EDC systems

Microsoft Office

Job description

Iterative Health is seeking a Clinical Research Coordinator I to support day-to-day trial activities, ensure protocol compliance, and safeguard patient safety across GI, hepatology, obesity, and cardiology studies. You will work with sponsors, CROs, investigators, and internal teams to deliver high-quality clinical research and patient experiences.

Responsibilities include coordinating visits, procedures, data entry, maintaining study documents, assisting with recruitment, and ensuring