Independent Clinical Research Coordinator II

Iterative Health; Providence (RI); On-site; USD 70,000 - 95,000; Full time

Job summary

Iterative Health is seeking a Clinical Research Coordinator II to independently coordinate daily study activities and ensure protocol compliance, safety, and data integrity. You will work with patients, investigators, sponsors, CROs, and internal teams to drive enrollment and high-quality trial execution.

The role requires a scientific/healthcare degree, 3–5 years of clinical research experience, and familiarity with CTMS/EDC systems, with opportunities to mentor junior staff and contribute to

Qualifications

• Associate’s or Bachelor’s degree in a scientific, healthcare, or related discipline required.
• 3-5 years of clinical research or healthcare experience required.
• Experience in gastroenterology, hepatology, or cardiology preferred.
• CCR C/C CRP or equivalent certification preferred.
• Proficiency with CTMS, EDC systems, and standard office software applications.

Responsibilities

• Coordinate industry-sponsored clinical trials from start-up through closeout with minimal supervision.
• Manage complex visit schedules and protocol-related activities to adhere to timelines.
• Lead patient recruitment and retention efforts, including consent discussions and enrollment tracking.
• Conduct patient visits and assessments in accordance with study protocols and GCP guidelines.
• Maintain accurate study documentation and timely data entry; support monitoring visits and inspections.

Skills

Organizational skills

Attention to detail

Prioritization

Reading protocols

Education

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

Tools

CTMS

EDC systems

Job description

Iterative Health is seeking a Clinical Research Coordinator II to independently coordinate daily study activities and ensure protocol compliance, safety, and data integrity. You will work with patients, investigators, sponsors, CROs, and internal teams to drive enrollment and high-quality trial execution.

The role requires a scientific/healthcare degree, 3–5 years of clinical research experience, and familiarity with CTMS/EDC systems, with opportunities to mentor junior staff and contribute to