Clinical Research Coordinator I: Drive Patient-Centered Trials

Iterative Health; Providence (RI); On-site; USD 60,000 - 80,000; Full time

Job summary

Iterative Health is seeking a Clinical Research Coordinator I (CRC I) to assist in day-to-day study activities and clinical trial execution across multiple sites. You will support patient visits, data collection, and regulatory documentation while ensuring patient safety and protocol compliance.

The role involves collaboration with sponsors, CROs, investigators, and internal teams to deliver high-quality research and advance innovative therapies in a fast-paced environment.

Qualifications

• Requires an Associate's or Bachelor's degree in a scientific, healthcare, or related discipline.
• 1–3 years of clinical research or healthcare experience.
• Ability to perform blood draws, EKGs, and basic vitals as applicable by state law.

Responsibilities

• Coordinate patient visits, procedures, and study activities per protocol and timelines.
• Support patient recruitment and retention through chart review, outreach, scheduling, and consent coordination.
• Maintain accurate study documentation and assist with data queries and regulatory monitoring preparations.

Skills

Blood draw

EKG

Data entry

Organizational skills

Protocol interpretation

Prioritization

CTMS/EDC familiarity

Education

Associate's or Bachelor's degree in a scientific/healthcare field

Tools

Microsoft Office

CTMS

EDC systems

Job description

Iterative Health is seeking a Clinical Research Coordinator I (CRC I) to assist in day-to-day study activities and clinical trial execution across multiple sites. You will support patient visits, data collection, and regulatory documentation while ensuring patient safety and protocol compliance.

The role involves collaboration with sponsors, CROs, investigators, and internal teams to deliver high-quality research and advance innovative therapies in a fast-paced environment.