Clinical Research Coordinator II — Trial Lead & Enrollment

Iterative Health; Dallas (TX); On-site; USD 65,000 - 90,000; Full time

Job summary

Iterative Health is seeking a Clinical Research Coordinator II to independently coordinate daily trial activities, ensure protocol compliance, and maintain patient safety guidelines across multiple sites.

You will lead patient recruitment, manage visit schedules, and collaborate with sponsors, CROs, and internal teams to optimize study execution and enrollment success. Strong regulatory knowledge and CTMS/EDC proficiency are valued.

Qualifications

• Associate’s or Bachelor’s degree in a scientific, healthcare, or related discipline.
• 3–5 years of clinical research or healthcare experience.
• Experience in gastroenterology, hepatology, or cardiology preferred.
• Certification (CCRC/CCRP) preferred.

Responsibilities

• Coordinate industry-sponsored clinical trials from start-up to closeout with minimal supervision.
• Manage complex visit schedules and protocol activities.
• Lead patient recruitment and retention, including informed consent discussions and enrollment tracking.
• Conduct protocol-required visits and procedures per GCP and site SOPs.
• Maintain study documentation and ensure data quality and timely resolution of data queries.
• Support monitoring visits, audits, and inspections.

Skills

Clinical research

GCP compliance

Enrollment coordination

Communication

Organizational skills

Education

Associate’s or Bachelor’s degree in a scientific/healthcare discipline

Tools

CTMS

EDC systems

Office software

Job description

Iterative Health is seeking a Clinical Research Coordinator II to independently coordinate daily trial activities, ensure protocol compliance, and maintain patient safety guidelines across multiple sites.

You will lead patient recruitment, manage visit schedules, and collaborate with sponsors, CROs, and internal teams to optimize study execution and enrollment success. Strong regulatory knowledge and CTMS/EDC proficiency are valued.