Clinical Research Coordinator II - Lead Complex Trials

Iterative-Health; Providence (RI); On-site; USD 65,000 - 90,000; Full time

Job summary

Iterative Health is a healthcare technology and services company driving the execution of clinical trials to improve patient outcomes.

As a Clinical Research Coordinator II, you will independently manage industry-sponsored studies, coordinate visits, and ensure protocol compliance while collaborating with sponsors, CROs, and internal teams to drive enrollment success and high-quality data.

Qualifications

• Associate’s or Bachelor’s degree required.
• 3–5 years of clinical research or healthcare experience required.
• Experience in gastroenterology, hepatology, or cardiology preferred.
• CCRC® or CCRP® or equivalent certification preferred.
• Proficiency with CTMS, EDC systems, and standard office software.

Responsibilities

• Coordinate industry-sponsored clinical trials from start-up through closeout with minimal supervision.
• Manage complex visit schedules and protocol-related activities.
• Lead patient recruitment and enrollment tracking to support study goals.
• Conduct protocol-required visits and assessments per GCP and SOPs.
• Maintain study documentation, data entry, and regulatory records; support monitoring visits.

Skills

Clinical research coordination

CTMS/EDC proficiency

Regulatory compliance

Data management

Communication skills

Education

Associate degree

Bachelor's degree

Tools

CTMS

EDC

Microsoft Office

Job description

Iterative Health is a healthcare technology and services company driving the execution of clinical trials to improve patient outcomes.

As a Clinical Research Coordinator II, you will independently manage industry-sponsored studies, coordinate visits, and ensure protocol compliance while collaborating with sponsors, CROs, and internal teams to drive enrollment success and high-quality data.