Clinical Research Coordinator II: Lead Trials & Care

Iterative Health; United States; Remote; USD 60,000 - 80,000; Full time

Job summary

Iterative Health is seeking a Clinical Research Coordinator II to independently coordinate daily study activities across GI, hepatology, obesity, and cardiology trials, ensuring protocol compliance and patient safety.

You will collaborate with investigators, sponsors, CROs, and internal teams to drive patient recruitment, data quality, and regulatory readiness while maintaining CTMS/EDC documentation and adherence to GCP, HIPAA, and SOPs.

Qualifications

• Associate’s or Bachelor’s degree in science, healthcare, or related field required.
• 3–5 years of clinical research or healthcare experience required.
• CCRC® or CCRP® certification preferred.
• Experience with CTMS/EDC systems preferred.

Responsibilities

• Coordinate industry-sponsored trials from start-up to closeout with minimal supervision.
• Manage complex visit schedules and protocol activities to meet timelines.
• Lead patient recruitment and retention including informed consent.
• Conduct protocol visits and essential procedures per GCP and SOPs.
• Ensure accurate study documentation and data entry.
• Prepare for sponsor and regulatory monitoring visits.
• Maintain inventory of study equipment and supplies.

Skills

Strong organizational skills

Attention to detail

Time management

Prioritization

Education

Associate’s or Bachelor’s degree in science/healthcare

Tools

CTMS

EDC systems

Office software

Job description

Iterative Health is seeking a Clinical Research Coordinator II to independently coordinate daily study activities across GI, hepatology, obesity, and cardiology trials, ensuring protocol compliance and patient safety.

You will collaborate with investigators, sponsors, CROs, and internal teams to drive patient recruitment, data quality, and regulatory readiness while maintaining CTMS/EDC documentation and adherence to GCP, HIPAA, and SOPs.