Clinical Research Coordinator II — Driving Trial Excellence

Iterative-Health; Mansfield (TX); On-site; USD 60,000 - 80,000; Full time

Job summary

Iterative Health is seeking a Clinical Research Coordinator II in Mansfield, TX to independently coordinate industry-sponsored trials from start-up through closeout, ensuring protocol adherence and patient safety. You will partner with investigators, sponsors, CROs, and internal teams to drive enrollment, data accuracy, and study quality.

The role requires 3–5 years in clinical research, a science/healthcare degree, and experience with CTMS/EDC systems.

Qualifications

• Requires an Associate’s or Bachelor's degree in a scientific, healthcare, or related field.
• 3–5 years of clinical research or healthcare experience.
• Experience in gastroenterology, hepatology, or cardiology is preferred.
• CCRC® or CCRP® certification preferred.
• Proficiency with CTMS and EDC systems.

Responsibilities

• Independently coordinate and manage industry-sponsored clinical trials from start-up through closeout with minimal supervision.
• 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.
• Review safety reports and ensure appropriate investigator review and documentation in a timely manner.
• Maintain accurate, complete, and timely study documentation including source records and CTMS updates.

Skills

Organizational skills

Attention to detail

Prioritization

Communication

Education

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

Tools

CTMS

EDC systems

Office software

Job description

Iterative Health is seeking a Clinical Research Coordinator II in Mansfield, TX to independently coordinate industry-sponsored trials from start-up through closeout, ensuring protocol adherence and patient safety. You will partner with investigators, sponsors, CROs, and internal teams to drive enrollment, data accuracy, and study quality.

The role requires 3–5 years in clinical research, a science/healthcare degree, and experience with CTMS/EDC systems.