Clinical Research Coordinator I: Accelerating Trials & Patient Care

Iterative Health; Providence (RI); On-site; USD 52,000 - 76,000; Full time

Job summary

Iterative Health is seeking a Clinical Research Coordinator I (CRC I) to support the execution of industry-sponsored trials, ensure protocol compliance, and safeguard patient safety. You will work with sponsors, CROs, investigators, and internal teams to deliver high-quality clinical research.

Ideal candidates have an Associate’s or Bachelor’s degree in a scientific or healthcare field and 1–3 years of clinical research or healthcare experience.

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.
• Ability to perform blood draws, vital signs, and EKGs under applicable regulations.

Responsibilities

• Support coordination and execution of industry-sponsored clinical trials under leadership guidance.
• Coordinate patient visits, procedures, and study-related activities per protocol and timelines.
• Assist with patient recruitment, outreach, scheduling, and informed consent coordination.
• Conduct protocol-required visits and assessments in line with GCP and site SOPs.
• Maintain accurate study documentation and ensure data entry quality.

Skills

Blood draw

EKGs

Regulatory knowledge

CTMS/EDC familiarity

Data entry

Education

Associate/Bachelor's degree in science/healthcare

Tools

CTMS/EDC systems

Job description

Iterative Health is seeking a Clinical Research Coordinator I (CRC I) to support the execution of industry-sponsored trials, ensure protocol compliance, and safeguard patient safety. You will work with sponsors, CROs, investigators, and internal teams to deliver high-quality clinical research.

Ideal candidates have an Associate’s or Bachelor’s degree in a scientific or healthcare field and 1–3 years of clinical research or healthcare experience.