Lead Clinical Research Coordinator — Multi-Site Trials

Iterative Health; Southlake (TX); On-site; USD 60,000 - 85,000; Full time

Job summary

Iterative Health is seeking a Clinical Research Coordinator II to oversee industry-sponsored trials across multiple sites. You will coordinate visits, ensure protocol compliance, and actively recruit and enroll participants while collaborating with sponsors, CROs, and internal teams.

The role requires 3–5 years in clinical research or healthcare, with a preference for gastroenterology/hepatology/cardiology and certification such as CCRC/CCRP.

Qualifications

• 3-5 years of clinical research or healthcare experience.
• Experience in gastroenterology, hepatology, or cardiology preferred.
• CCRC or CCRP certification preferred.

Responsibilities

• Independently coordinate industry-sponsored trials from start-up to closeout.
• Manage complex visit schedules and protocol activities to meet timelines.
• Lead patient recruitment, consent, and enrollment tracking.
• Conduct study visits and assessments per protocol and GCP.
• Maintain timely study documentation and data integrity.

Skills

Organizational skills

Attention to detail

Prioritization

Communication skills

Education

Associate’s degree

Bachelor’s degree in science

Tools

CTMS

EDC systems

Job description

Iterative Health is seeking a Clinical Research Coordinator II to oversee industry-sponsored trials across multiple sites. You will coordinate visits, ensure protocol compliance, and actively recruit and enroll participants while collaborating with sponsors, CROs, and internal teams.

The role requires 3–5 years in clinical research or healthcare, with a preference for gastroenterology/hepatology/cardiology and certification such as CCRC/CCRP.