Clinical Research Coordinator II: Lead Trial Execution

Iterative Scopes; Waterloo (IA); On-site; USD 60,000 - 90,000; Full time

Job summary

Iterative Health in the United States seeks a Clinical Research Coordinator II to independently coordinate daily study activities and ensure protocol compliance, regulatory standards, and patient safety.

You will manage complex industry-sponsored trials from start-up through closeout, lead patient recruitment and retention, and maintain rigorous study documentation in CTMS/EDC systems while collaborating with sponsors, CROs, investigators, and internal teams.

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.
• CCRC® or CCRP® certification preferred.
• Strong organizational skills and attention to detail.
• Proficiency with CTMS, EDC systems, and standard office software applications.

Responsibilities

• Independently coordinate and manage industry-sponsored clinical trials from study start‑up through closeout with minimal supervision.
• Manage complex study visit schedules and protocol-related activities while ensuring adherence to study timelines and requirements.
• Lead patient recruitment and retention efforts including chart review, patient outreach, informed consent discussions, and enrollment tracking to support study enrollment goals.
• Conduct protocol-required patient visits and assessments in accordance with study protocols, GCP guidelines, and site SOPs.
• Maintain accurate, complete, and timely study documentation including source records, informed consent forms, CTMS updates, and case report forms.

Skills

Clinical research

Data management

Study coordination

Regulatory compliance

CTMS / EDC familiarity

Education

Associate’s or Bachelor’s degree in scientific/healthcare field

Bachelor’s degree in sciences

Tools

CTMS

EDC systems

Job description

Iterative Health in the United States seeks a Clinical Research Coordinator II to independently coordinate daily study activities and ensure protocol compliance, regulatory standards, and patient safety.

You will manage complex industry-sponsored trials from start-up through closeout, lead patient recruitment and retention, and maintain rigorous study documentation in CTMS/EDC systems while collaborating with sponsors, CROs, investigators, and internal teams.