Clinical Research Coordinator II — Trial Lead

Iterative Scopes; Southlake (TX); On-site; USD 60,000 - 90,000; Full time

Job summary

Iterative Health is seeking a Clinical Research Coordinator II to independently coordinate daily study activities and ensure protocol compliance. You will manage complex trial visits, assist with recruitment and consent, and maintain meticulous source documents and data integrity, supporting the overall trial success.

The role requires 3–5 years of clinical research experience, familiarity with CTMS and EDC systems, and adherence to GCP and HIPAA guidelines.

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.
• CCRC® or CCRP® or equivalent certification preferred.
• Strong organizational skills and attention to detail.

Responsibilities

• Coordinate industry-sponsored clinical trials from start-up through closeout with minimal supervision.
• Manage study visit schedules and ensure adherence to timelines.
• Lead patient recruitment, outreach, consent discussions, and enrollment tracking.

Skills

Clinical research

CTMS/EDC proficiency

GCP compliance

Communication

Education

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

CCR P/CCRP or equivalent certification preferred

Tools

CTMS

EDC systems

Office software

Job description

Iterative Health is seeking a Clinical Research Coordinator II to independently coordinate daily study activities and ensure protocol compliance. You will manage complex trial visits, assist with recruitment and consent, and maintain meticulous source documents and data integrity, supporting the overall trial success.

The role requires 3–5 years of clinical research experience, familiarity with CTMS and EDC systems, and adherence to GCP and HIPAA guidelines.